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Select item 14915808461.

rs1491580846 has merged into rs201576721 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAGAAAAAAAAAAAAAAA,AAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAGAAAAAGAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:89726493 (GRCh38)
6:90436212 (GRCh37)
Canonical SPDI:: NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89726482:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAGAAAAAGAAAAAAAAAAAAAAA
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.16773/840 (1000Genomes)
-=0.2/8 (GENOME_DK)
HGVS:: NC_000006.12:g.89726493_89726496del, NC_000006.12:g.89726495_89726496del, NC_000006.12:g.89726496del, NC_000006.12:g.89726496dup, NC_000006.12:g.89726495_89726496dup, NC_000006.12:g.89726494_89726496dup, NC_000006.12:g.89726493_89726496dup, NC_000006.12:g.89726491_89726496dup, NC_000006.12:g.89726490_89726496dup, NC_000006.12:g.89726489_89726496dup, NC_000006.12:g.89726488_89726496dup, NC_000006.12:g.89726487_89726496dup, NC_000006.12:g.89726486_89726496dup, NC_000006.12:g.89726485_89726496dup, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726496_89726497insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89726483_89726496A[36]TAAAAAAAAAAAAAAAA[1], NC_000006.12:g.89726483_89726496A[35]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.89726483_89726496A[19]GAAAAAAAAAAAAAAA[1], NC_000006.12:g.89726483_89726496A[19]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.89726483_89726496A[18]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.89726483_89726496A[18]GAAAAA[2]A[10], NC_000006.11:g.90436212_90436215del, NC_000006.11:g.90436214_90436215del, NC_000006.11:g.90436215del, NC_000006.11:g.90436215dup, NC_000006.11:g.90436214_90436215dup, NC_000006.11:g.90436213_90436215dup, NC_000006.11:g.90436212_90436215dup, NC_000006.11:g.90436210_90436215dup, NC_000006.11:g.90436209_90436215dup, NC_000006.11:g.90436208_90436215dup, NC_000006.11:g.90436207_90436215dup, NC_000006.11:g.90436206_90436215dup, NC_000006.11:g.90436205_90436215dup, NC_000006.11:g.90436204_90436215dup, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436215_90436216insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90436202_90436215A[36]TAAAAAAAAAAAAAAAA[1], NC_000006.11:g.90436202_90436215A[35]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.90436202_90436215A[19]GAAAAAAAAAAAAAAA[1], NC_000006.11:g.90436202_90436215A[19]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.90436202_90436215A[18]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.90436202_90436215A[18]GAAAAA[2]A[10], NG_034012.1:g.98309_98312del, NG_034012.1:g.98311_98312del, NG_034012.1:g.98312del, NG_034012.1:g.98312dup, NG_034012.1:g.98311_98312dup, NG_034012.1:g.98310_98312dup, NG_034012.1:g.98309_98312dup, NG_034012.1:g.98307_98312dup, NG_034012.1:g.98306_98312dup, NG_034012.1:g.98305_98312dup, NG_034012.1:g.98304_98312dup, NG_034012.1:g.98303_98312dup, NG_034012.1:g.98302_98312dup, NG_034012.1:g.98301_98312dup, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98312_98313insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.98299_98312T[16]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_034012.1:g.98299_98312T[22]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_034012.1:g.98299_98312T[15]CTTTTTTTTTTTTTTTTTTT[1], NG_034012.1:g.98299_98312T[22]CTTTTTTTTTTTTTTTTTTT[1], NG_034012.1:g.98299_98312T[22]CTTTTTTTTTTTTTTTTTT[1], NG_034012.1:g.98299_98312T[15]CTTTTT[2]T[13]

Select item 14915734032.

rs1491573403 has merged into rs753013686 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:89824720 (GRCh38)
6:90534439 (GRCh37)
Canonical SPDI:: NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89824710:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
AA=0.375/15 (GENOME_DK)
HGVS:: NC_000006.12:g.89824720_89824732del, NC_000006.12:g.89824722_89824732del, NC_000006.12:g.89824723_89824732del, NC_000006.12:g.89824725_89824732del, NC_000006.12:g.89824726_89824732del, NC_000006.12:g.89824727_89824732del, NC_000006.12:g.89824728_89824732del, NC_000006.12:g.89824729_89824732del, NC_000006.12:g.89824730_89824732del, NC_000006.12:g.89824731_89824732del, NC_000006.12:g.89824732del, NC_000006.12:g.89824732dup, NC_000006.12:g.89824731_89824732dup, NC_000006.12:g.89824730_89824732dup, NC_000006.12:g.89824729_89824732dup, NC_000006.12:g.89824728_89824732dup, NC_000006.12:g.89824727_89824732dup, NC_000006.12:g.89824724_89824732dup, NC_000006.12:g.89824721_89824732dup, NC_000006.12:g.89824717_89824732dup, NC_000006.11:g.90534439_90534451del, NC_000006.11:g.90534441_90534451del, NC_000006.11:g.90534442_90534451del, NC_000006.11:g.90534444_90534451del, NC_000006.11:g.90534445_90534451del, NC_000006.11:g.90534446_90534451del, NC_000006.11:g.90534447_90534451del, NC_000006.11:g.90534448_90534451del, NC_000006.11:g.90534449_90534451del, NC_000006.11:g.90534450_90534451del, NC_000006.11:g.90534451del, NC_000006.11:g.90534451dup, NC_000006.11:g.90534450_90534451dup, NC_000006.11:g.90534449_90534451dup, NC_000006.11:g.90534448_90534451dup, NC_000006.11:g.90534447_90534451dup, NC_000006.11:g.90534446_90534451dup, NC_000006.11:g.90534443_90534451dup, NC_000006.11:g.90534440_90534451dup, NC_000006.11:g.90534436_90534451dup, NG_034012.1:g.72_84del, NG_034012.1:g.74_84del, NG_034012.1:g.75_84del, NG_034012.1:g.77_84del, NG_034012.1:g.78_84del, NG_034012.1:g.79_84del, NG_034012.1:g.80_84del, NG_034012.1:g.81_84del, NG_034012.1:g.82_84del, NG_034012.1:g.83_84del, NG_034012.1:g.84del, NG_034012.1:g.84dup, NG_034012.1:g.83_84dup, NG_034012.1:g.82_84dup, NG_034012.1:g.81_84dup, NG_034012.1:g.80_84dup, NG_034012.1:g.79_84dup, NG_034012.1:g.76_84dup, NG_034012.1:g.73_84dup, NG_034012.1:g.69_84dup, NW_017363815.1:g.20065_20077del, NW_017363815.1:g.20067_20077del, NW_017363815.1:g.20068_20077del, NW_017363815.1:g.20070_20077del, NW_017363815.1:g.20071_20077del, NW_017363815.1:g.20072_20077del, NW_017363815.1:g.20073_20077del, NW_017363815.1:g.20074_20077del, NW_017363815.1:g.20075_20077del, NW_017363815.1:g.20076_20077del, NW_017363815.1:g.20077del, NW_017363815.1:g.20077dup, NW_017363815.1:g.20076_20077dup, NW_017363815.1:g.20075_20077dup, NW_017363815.1:g.20074_20077dup, NW_017363815.1:g.20073_20077dup, NW_017363815.1:g.20072_20077dup, NW_017363815.1:g.20069_20077dup, NW_017363815.1:g.20066_20077dup, NW_017363815.1:g.20062_20077dup

Select item 14915726393.

rs1491572639 has merged into rs766450069 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:89670180 (GRCh38)
6:90379899 (GRCh37)
Canonical SPDI:: NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:89670170:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MDN1 (Varview), MDN1-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
TTTTTTTTTT=0.03115/675 (TOMMO)
TTTTTTT=0.125/5 (GENOME_DK)
HGVS:: NC_000006.12:g.89670180_89670190del, NC_000006.12:g.89670181_89670190del, NC_000006.12:g.89670182_89670190del, NC_000006.12:g.89670183_89670190del, NC_000006.12:g.89670184_89670190del, NC_000006.12:g.89670185_89670190del, NC_000006.12:g.89670186_89670190del, NC_000006.12:g.89670187_89670190del, NC_000006.12:g.89670188_89670190del, NC_000006.12:g.89670189_89670190del, NC_000006.12:g.89670190del, NC_000006.12:g.89670190dup, NC_000006.12:g.89670189_89670190dup, NC_000006.12:g.89670188_89670190dup, NC_000006.12:g.89670187_89670190dup, NC_000006.12:g.89670186_89670190dup, NC_000006.12:g.89670185_89670190dup, NC_000006.12:g.89670184_89670190dup, NC_000006.12:g.89670183_89670190dup, NC_000006.12:g.89670182_89670190dup, NC_000006.12:g.89670181_89670190dup, NC_000006.12:g.89670180_89670190dup, NC_000006.12:g.89670179_89670190dup, NC_000006.12:g.89670178_89670190dup, NC_000006.12:g.89670177_89670190dup, NC_000006.12:g.89670176_89670190dup, NC_000006.12:g.89670175_89670190dup, NC_000006.11:g.90379899_90379909del, NC_000006.11:g.90379900_90379909del, NC_000006.11:g.90379901_90379909del, NC_000006.11:g.90379902_90379909del, NC_000006.11:g.90379903_90379909del, NC_000006.11:g.90379904_90379909del, NC_000006.11:g.90379905_90379909del, NC_000006.11:g.90379906_90379909del, NC_000006.11:g.90379907_90379909del, NC_000006.11:g.90379908_90379909del, NC_000006.11:g.90379909del, NC_000006.11:g.90379909dup, NC_000006.11:g.90379908_90379909dup, NC_000006.11:g.90379907_90379909dup, NC_000006.11:g.90379906_90379909dup, NC_000006.11:g.90379905_90379909dup, NC_000006.11:g.90379904_90379909dup, NC_000006.11:g.90379903_90379909dup, NC_000006.11:g.90379902_90379909dup, NC_000006.11:g.90379901_90379909dup, NC_000006.11:g.90379900_90379909dup, NC_000006.11:g.90379899_90379909dup, NC_000006.11:g.90379898_90379909dup, NC_000006.11:g.90379897_90379909dup, NC_000006.11:g.90379896_90379909dup, NC_000006.11:g.90379895_90379909dup, NC_000006.11:g.90379894_90379909dup, NG_034012.1:g.154614_154624del, NG_034012.1:g.154615_154624del, NG_034012.1:g.154616_154624del, NG_034012.1:g.154617_154624del, NG_034012.1:g.154618_154624del, NG_034012.1:g.154619_154624del, NG_034012.1:g.154620_154624del, NG_034012.1:g.154621_154624del, NG_034012.1:g.154622_154624del, NG_034012.1:g.154623_154624del, NG_034012.1:g.154624del, NG_034012.1:g.154624dup, NG_034012.1:g.154623_154624dup, NG_034012.1:g.154622_154624dup, NG_034012.1:g.154621_154624dup, NG_034012.1:g.154620_154624dup, NG_034012.1:g.154619_154624dup, NG_034012.1:g.154618_154624dup, NG_034012.1:g.154617_154624dup, NG_034012.1:g.154616_154624dup, NG_034012.1:g.154615_154624dup, NG_034012.1:g.154614_154624dup, NG_034012.1:g.154613_154624dup, NG_034012.1:g.154612_154624dup, NG_034012.1:g.154611_154624dup, NG_034012.1:g.154610_154624dup, NG_034012.1:g.154609_154624dup

Select item 14915596394.

rs1491559639 has merged into rs61558155 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:89810005 (GRCh38)
6:90519724 (GRCh37)
Canonical SPDI:: NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89809993:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000006.12:g.89810005_89810026del, NC_000006.12:g.89810008_89810026del, NC_000006.12:g.89810009_89810026del, NC_000006.12:g.89810010_89810026del, NC_000006.12:g.89810011_89810026del, NC_000006.12:g.89810012_89810026del, NC_000006.12:g.89810013_89810026del, NC_000006.12:g.89810014_89810026del, NC_000006.12:g.89810015_89810026del, NC_000006.12:g.89810016_89810026del, NC_000006.12:g.89810017_89810026del, NC_000006.12:g.89810018_89810026del, NC_000006.12:g.89810019_89810026del, NC_000006.12:g.89810020_89810026del, NC_000006.12:g.89810021_89810026del, NC_000006.12:g.89810022_89810026del, NC_000006.12:g.89810023_89810026del, NC_000006.12:g.89810024_89810026del, NC_000006.12:g.89810025_89810026del, NC_000006.12:g.89810026del, NC_000006.12:g.89810026dup, NC_000006.12:g.89810025_89810026dup, NC_000006.12:g.89810024_89810026dup, NC_000006.12:g.89810023_89810026dup, NC_000006.12:g.89810022_89810026dup, NC_000006.12:g.89810021_89810026dup, NC_000006.12:g.89810020_89810026dup, NC_000006.12:g.89810019_89810026dup, NC_000006.12:g.89810018_89810026dup, NC_000006.11:g.90519724_90519745del, NC_000006.11:g.90519727_90519745del, NC_000006.11:g.90519728_90519745del, NC_000006.11:g.90519729_90519745del, NC_000006.11:g.90519730_90519745del, NC_000006.11:g.90519731_90519745del, NC_000006.11:g.90519732_90519745del, NC_000006.11:g.90519733_90519745del, NC_000006.11:g.90519734_90519745del, NC_000006.11:g.90519735_90519745del, NC_000006.11:g.90519736_90519745del, NC_000006.11:g.90519737_90519745del, NC_000006.11:g.90519738_90519745del, NC_000006.11:g.90519739_90519745del, NC_000006.11:g.90519740_90519745del, NC_000006.11:g.90519741_90519745del, NC_000006.11:g.90519742_90519745del, NC_000006.11:g.90519743_90519745del, NC_000006.11:g.90519744_90519745del, NC_000006.11:g.90519745del, NC_000006.11:g.90519745dup, NC_000006.11:g.90519744_90519745dup, NC_000006.11:g.90519743_90519745dup, NC_000006.11:g.90519742_90519745dup, NC_000006.11:g.90519741_90519745dup, NC_000006.11:g.90519740_90519745dup, NC_000006.11:g.90519739_90519745dup, NC_000006.11:g.90519738_90519745dup, NC_000006.11:g.90519737_90519745dup, NG_034012.1:g.14780_14801del, NG_034012.1:g.14783_14801del, NG_034012.1:g.14784_14801del, NG_034012.1:g.14785_14801del, NG_034012.1:g.14786_14801del, NG_034012.1:g.14787_14801del, NG_034012.1:g.14788_14801del, NG_034012.1:g.14789_14801del, NG_034012.1:g.14790_14801del, NG_034012.1:g.14791_14801del, NG_034012.1:g.14792_14801del, NG_034012.1:g.14793_14801del, NG_034012.1:g.14794_14801del, NG_034012.1:g.14795_14801del, NG_034012.1:g.14796_14801del, NG_034012.1:g.14797_14801del, NG_034012.1:g.14798_14801del, NG_034012.1:g.14799_14801del, NG_034012.1:g.14800_14801del, NG_034012.1:g.14801del, NG_034012.1:g.14801dup, NG_034012.1:g.14800_14801dup, NG_034012.1:g.14799_14801dup, NG_034012.1:g.14798_14801dup, NG_034012.1:g.14797_14801dup, NG_034012.1:g.14796_14801dup, NG_034012.1:g.14795_14801dup, NG_034012.1:g.14794_14801dup, NG_034012.1:g.14793_14801dup, NW_017363815.1:g.5350_5371del, NW_017363815.1:g.5353_5371del, NW_017363815.1:g.5354_5371del, NW_017363815.1:g.5355_5371del, NW_017363815.1:g.5356_5371del, NW_017363815.1:g.5357_5371del, NW_017363815.1:g.5358_5371del, NW_017363815.1:g.5359_5371del, NW_017363815.1:g.5360_5371del, NW_017363815.1:g.5361_5371del, NW_017363815.1:g.5362_5371del, NW_017363815.1:g.5363_5371del, NW_017363815.1:g.5364_5371del, NW_017363815.1:g.5365_5371del, NW_017363815.1:g.5366_5371del, NW_017363815.1:g.5367_5371del, NW_017363815.1:g.5368_5371del, NW_017363815.1:g.5369_5371del, NW_017363815.1:g.5370_5371del, NW_017363815.1:g.5371del, NW_017363815.1:g.5371dup, NW_017363815.1:g.5370_5371dup, NW_017363815.1:g.5369_5371dup, NW_017363815.1:g.5368_5371dup, NW_017363815.1:g.5367_5371dup, NW_017363815.1:g.5366_5371dup, NW_017363815.1:g.5365_5371dup, NW_017363815.1:g.5364_5371dup, NW_017363815.1:g.5363_5371dup

Select item 14915534955.

rs1491553495 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 6:89811095 (GRCh38)
6:90520814 (GRCh37)
Canonical SPDI:: NC_000006.12:89811091:TATAT:TAT
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TAT=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.89811093AT[1], NC_000006.11:g.90520812AT[1], NG_034012.1:g.13700TA[1], NW_017363815.1:g.6438AT[1]

Select item 14915526116.

rs1491552611 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 6:89670140 (GRCh38)
6:90379860 (GRCh37)
Canonical SPDI:: NC_000006.12:89670140:T:TT
Gene:: MDN1 (Varview), MDN1-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.00003/1 (GnomAD)
HGVS:: NC_000006.12:g.89670141dup, NC_000006.11:g.90379860dup, NG_034012.1:g.154654dup

Select item 14915307947.

rs1491530794 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:89786924 (GRCh38)
6:90496643 (GRCh37)
Canonical SPDI:: NC_000006.12:89786923:CA:
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.03052/362 (ALFA)
-=0.0026/91 (GnomAD)
-=0.0089/246 (TOMMO)
HGVS:: NC_000006.12:g.89786924_89786925del, NC_000006.11:g.90496643_90496644del, NG_034012.1:g.37870_37871del

Select item 14915193878.

rs1491519387 has merged into rs35077997 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:89786935 (GRCh38)
6:90496654 (GRCh37)
Canonical SPDI:: NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89786924:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000006.12:g.89786935_89786947del, NC_000006.12:g.89786939_89786947del, NC_000006.12:g.89786940_89786947del, NC_000006.12:g.89786941_89786947del, NC_000006.12:g.89786942_89786947del, NC_000006.12:g.89786943_89786947del, NC_000006.12:g.89786944_89786947del, NC_000006.12:g.89786945_89786947del, NC_000006.12:g.89786946_89786947del, NC_000006.12:g.89786947del, NC_000006.12:g.89786947dup, NC_000006.12:g.89786946_89786947dup, NC_000006.12:g.89786945_89786947dup, NC_000006.12:g.89786944_89786947dup, NC_000006.12:g.89786943_89786947dup, NC_000006.12:g.89786942_89786947dup, NC_000006.12:g.89786940_89786947dup, NC_000006.12:g.89786932_89786947dup, NC_000006.11:g.90496654_90496666del, NC_000006.11:g.90496658_90496666del, NC_000006.11:g.90496659_90496666del, NC_000006.11:g.90496660_90496666del, NC_000006.11:g.90496661_90496666del, NC_000006.11:g.90496662_90496666del, NC_000006.11:g.90496663_90496666del, NC_000006.11:g.90496664_90496666del, NC_000006.11:g.90496665_90496666del, NC_000006.11:g.90496666del, NC_000006.11:g.90496666dup, NC_000006.11:g.90496665_90496666dup, NC_000006.11:g.90496664_90496666dup, NC_000006.11:g.90496663_90496666dup, NC_000006.11:g.90496662_90496666dup, NC_000006.11:g.90496661_90496666dup, NC_000006.11:g.90496659_90496666dup, NC_000006.11:g.90496651_90496666dup, NG_034012.1:g.37858_37870del, NG_034012.1:g.37862_37870del, NG_034012.1:g.37863_37870del, NG_034012.1:g.37864_37870del, NG_034012.1:g.37865_37870del, NG_034012.1:g.37866_37870del, NG_034012.1:g.37867_37870del, NG_034012.1:g.37868_37870del, NG_034012.1:g.37869_37870del, NG_034012.1:g.37870del, NG_034012.1:g.37870dup, NG_034012.1:g.37869_37870dup, NG_034012.1:g.37868_37870dup, NG_034012.1:g.37867_37870dup, NG_034012.1:g.37866_37870dup, NG_034012.1:g.37865_37870dup, NG_034012.1:g.37863_37870dup, NG_034012.1:g.37855_37870dup

Select item 14915032989.

rs1491503298 has merged into rs10706907 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:89798186 (GRCh38)
6:90507905 (GRCh37)
Canonical SPDI:: NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89798181:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0./0 (ALFA)
-=0.0576/222 (ALSPAC)
HGVS:: NC_000006.12:g.89798186_89798202del, NC_000006.12:g.89798187_89798202del, NC_000006.12:g.89798189_89798202del, NC_000006.12:g.89798190_89798202del, NC_000006.12:g.89798191_89798202del, NC_000006.12:g.89798192_89798202del, NC_000006.12:g.89798193_89798202del, NC_000006.12:g.89798194_89798202del, NC_000006.12:g.89798195_89798202del, NC_000006.12:g.89798196_89798202del, NC_000006.12:g.89798197_89798202del, NC_000006.12:g.89798198_89798202del, NC_000006.12:g.89798199_89798202del, NC_000006.12:g.89798200_89798202del, NC_000006.12:g.89798201_89798202del, NC_000006.12:g.89798202del, NC_000006.12:g.89798202dup, NC_000006.12:g.89798201_89798202dup, NC_000006.12:g.89798200_89798202dup, NC_000006.12:g.89798199_89798202dup, NC_000006.12:g.89798198_89798202dup, NC_000006.12:g.89798197_89798202dup, NC_000006.12:g.89798196_89798202dup, NC_000006.12:g.89798195_89798202dup, NC_000006.12:g.89798194_89798202dup, NC_000006.12:g.89798193_89798202dup, NC_000006.12:g.89798190_89798202dup, NC_000006.11:g.90507905_90507921del, NC_000006.11:g.90507906_90507921del, NC_000006.11:g.90507908_90507921del, NC_000006.11:g.90507909_90507921del, NC_000006.11:g.90507910_90507921del, NC_000006.11:g.90507911_90507921del, NC_000006.11:g.90507912_90507921del, NC_000006.11:g.90507913_90507921del, NC_000006.11:g.90507914_90507921del, NC_000006.11:g.90507915_90507921del, NC_000006.11:g.90507916_90507921del, NC_000006.11:g.90507917_90507921del, NC_000006.11:g.90507918_90507921del, NC_000006.11:g.90507919_90507921del, NC_000006.11:g.90507920_90507921del, NC_000006.11:g.90507921del, NC_000006.11:g.90507921dup, NC_000006.11:g.90507920_90507921dup, NC_000006.11:g.90507919_90507921dup, NC_000006.11:g.90507918_90507921dup, NC_000006.11:g.90507917_90507921dup, NC_000006.11:g.90507916_90507921dup, NC_000006.11:g.90507915_90507921dup, NC_000006.11:g.90507914_90507921dup, NC_000006.11:g.90507913_90507921dup, NC_000006.11:g.90507912_90507921dup, NC_000006.11:g.90507909_90507921dup, NG_034012.1:g.26597_26613del, NG_034012.1:g.26598_26613del, NG_034012.1:g.26600_26613del, NG_034012.1:g.26601_26613del, NG_034012.1:g.26602_26613del, NG_034012.1:g.26603_26613del, NG_034012.1:g.26604_26613del, NG_034012.1:g.26605_26613del, NG_034012.1:g.26606_26613del, NG_034012.1:g.26607_26613del, NG_034012.1:g.26608_26613del, NG_034012.1:g.26609_26613del, NG_034012.1:g.26610_26613del, NG_034012.1:g.26611_26613del, NG_034012.1:g.26612_26613del, NG_034012.1:g.26613del, NG_034012.1:g.26613dup, NG_034012.1:g.26612_26613dup, NG_034012.1:g.26611_26613dup, NG_034012.1:g.26610_26613dup, NG_034012.1:g.26609_26613dup, NG_034012.1:g.26608_26613dup, NG_034012.1:g.26607_26613dup, NG_034012.1:g.26606_26613dup, NG_034012.1:g.26605_26613dup, NG_034012.1:g.26604_26613dup, NG_034012.1:g.26601_26613dup

Select item 149150065310.

rs1491500653 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 6:89722847 (GRCh38)
6:90432567 (GRCh37)
Canonical SPDI:: NC_000006.12:89722847::C
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/1 (GnomAD)
HGVS:: NC_000006.12:g.89722847_89722848insC, NC_000006.11:g.90432566_90432567insC, NG_034012.1:g.101947_101948insG

Select item 149149299211.

rs1491492992 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:89809215 (GRCh38)
6:90518934 (GRCh37)
Canonical SPDI:: NC_000006.12:89809214:CA:
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.89809215_89809216del, NC_000006.11:g.90518934_90518935del, NG_034012.1:g.15579_15580del, NW_017363815.1:g.4560_4561del

Select item 149148615312.

rs1491486153 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 6:89776075 (GRCh38)
6:90485794 (GRCh37)
Canonical SPDI:: NC_000006.12:89776073:ATA:A
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
-=0.000019/5 (TOPMED)
HGVS:: NC_000006.12:g.89776075_89776076del, NC_000006.11:g.90485794_90485795del, NG_034012.1:g.48720_48721del

Select item 149147226013.

rs1491472260 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:89824710 (GRCh38)
6:90534429 (GRCh37)
Canonical SPDI:: NC_000006.12:89824709:CA:
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.89824710_89824711del, NC_000006.11:g.90534429_90534430del, NG_034012.1:g.84_85del, NW_017363815.1:g.20055_20056del

Select item 149146784514.

rs1491467845 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAAAAAGAAAAAAAAAAAAA,AAAAAGAAAAAAAAAAAAA,AAAAGAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:89726483 (GRCh38)
6:90436203 (GRCh37)
Canonical SPDI:: NC_000006.12:89726483:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAA,NC_000006.12:89726483:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAA,NC_000006.12:89726483:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAGAAAAAAAAAAAAA
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: AAAAAAAAAAAAAAAAAG=0.00006/1 (TOMMO)
HGVS:: NC_000006.12:g.89726484_89726496A[19]GAAAAAAAAAAAAA[1], NC_000006.12:g.89726484_89726496A[18]GAAAAAAAAAAAAA[1], NC_000006.12:g.89726484_89726496A[17]GAAAAAAAAAAAAA[1], NC_000006.11:g.90436203_90436215A[19]GAAAAAAAAAAAAA[1], NC_000006.11:g.90436203_90436215A[18]GAAAAAAAAAAAAA[1], NC_000006.11:g.90436203_90436215A[17]GAAAAAAAAAAAAA[1], NG_034012.1:g.98299_98311T[13]CTTTTTTTTTTTTTTTTTTT[1], NG_034012.1:g.98299_98311T[13]CTTTTTTTTTTTTTTTTTT[1], NG_034012.1:g.98299_98311T[13]CTTTTTTTTTTTTTTTTT[1]

Select item 149146073215.

rs1491460732 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:89651324 (GRCh38)
6:90361043 (GRCh37)
Canonical SPDI:: NC_000006.12:89651323:CA:
Gene:: MDN1 (Varview), MDN1-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00084/10 (ALFA)
HGVS:: NC_000006.12:g.89651324_89651325del, NC_000006.11:g.90361043_90361044del, NG_034012.1:g.173470_173471del

Select item 149144694916.

rs1491446949 has merged into rs11371433 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:89725749 (GRCh38)
6:90435468 (GRCh37)
Canonical SPDI:: NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:89725740:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.433307/2170 (1000Genomes)
HGVS:: NC_000006.12:g.89725749_89725756del, NC_000006.12:g.89725751_89725756del, NC_000006.12:g.89725752_89725756del, NC_000006.12:g.89725754_89725756del, NC_000006.12:g.89725755_89725756del, NC_000006.12:g.89725756del, NC_000006.12:g.89725756dup, NC_000006.12:g.89725755_89725756dup, NC_000006.12:g.89725754_89725756dup, NC_000006.12:g.89725753_89725756dup, NC_000006.12:g.89725751_89725756dup, NC_000006.11:g.90435468_90435475del, NC_000006.11:g.90435470_90435475del, NC_000006.11:g.90435471_90435475del, NC_000006.11:g.90435473_90435475del, NC_000006.11:g.90435474_90435475del, NC_000006.11:g.90435475del, NC_000006.11:g.90435475dup, NC_000006.11:g.90435474_90435475dup, NC_000006.11:g.90435473_90435475dup, NC_000006.11:g.90435472_90435475dup, NC_000006.11:g.90435470_90435475dup, NG_034012.1:g.99047_99054del, NG_034012.1:g.99049_99054del, NG_034012.1:g.99050_99054del, NG_034012.1:g.99052_99054del, NG_034012.1:g.99053_99054del, NG_034012.1:g.99054del, NG_034012.1:g.99054dup, NG_034012.1:g.99053_99054dup, NG_034012.1:g.99052_99054dup, NG_034012.1:g.99051_99054dup, NG_034012.1:g.99049_99054dup

Select item 149144044917.

rs1491440449 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGT [Show Flanks]
Chromosome:: 6:89776074 (GRCh38)
6:90485794 (GRCh37)
Canonical SPDI:: NC_000006.12:89776074:TAGT:TAGTAGT
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TAGTAGT=0./0 (ALFA)
TAG=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.89776076_89776078dup, NC_000006.11:g.90485795_90485797dup, NG_034012.1:g.48718_48720dup

Select item 149143728018.

rs1491437280 has merged into rs55885838 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:89747900 (GRCh38)
6:90457619 (GRCh37)
Canonical SPDI:: NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:89747890:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
A=0.406/2033 (1000Genomes)
A=0.425/17 (GENOME_DK)
HGVS:: NC_000006.12:g.89747900_89747912del, NC_000006.12:g.89747901_89747912del, NC_000006.12:g.89747902_89747912del, NC_000006.12:g.89747903_89747912del, NC_000006.12:g.89747905_89747912del, NC_000006.12:g.89747906_89747912del, NC_000006.12:g.89747907_89747912del, NC_000006.12:g.89747908_89747912del, NC_000006.12:g.89747909_89747912del, NC_000006.12:g.89747910_89747912del, NC_000006.12:g.89747911_89747912del, NC_000006.12:g.89747912del, NC_000006.12:g.89747912dup, NC_000006.12:g.89747911_89747912dup, NC_000006.12:g.89747910_89747912dup, NC_000006.12:g.89747909_89747912dup, NC_000006.12:g.89747908_89747912dup, NC_000006.12:g.89747907_89747912dup, NC_000006.12:g.89747905_89747912dup, NC_000006.12:g.89747912_89747913insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.89747912_89747913insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90457619_90457631del, NC_000006.11:g.90457620_90457631del, NC_000006.11:g.90457621_90457631del, NC_000006.11:g.90457622_90457631del, NC_000006.11:g.90457624_90457631del, NC_000006.11:g.90457625_90457631del, NC_000006.11:g.90457626_90457631del, NC_000006.11:g.90457627_90457631del, NC_000006.11:g.90457628_90457631del, NC_000006.11:g.90457629_90457631del, NC_000006.11:g.90457630_90457631del, NC_000006.11:g.90457631del, NC_000006.11:g.90457631dup, NC_000006.11:g.90457630_90457631dup, NC_000006.11:g.90457629_90457631dup, NC_000006.11:g.90457628_90457631dup, NC_000006.11:g.90457627_90457631dup, NC_000006.11:g.90457626_90457631dup, NC_000006.11:g.90457624_90457631dup, NC_000006.11:g.90457631_90457632insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.90457631_90457632insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_034012.1:g.76892_76904del, NG_034012.1:g.76893_76904del, NG_034012.1:g.76894_76904del, NG_034012.1:g.76895_76904del, NG_034012.1:g.76897_76904del, NG_034012.1:g.76898_76904del, NG_034012.1:g.76899_76904del, NG_034012.1:g.76900_76904del, NG_034012.1:g.76901_76904del, NG_034012.1:g.76902_76904del, NG_034012.1:g.76903_76904del, NG_034012.1:g.76904del, NG_034012.1:g.76904dup, NG_034012.1:g.76903_76904dup, NG_034012.1:g.76902_76904dup, NG_034012.1:g.76901_76904dup, NG_034012.1:g.76900_76904dup, NG_034012.1:g.76899_76904dup, NG_034012.1:g.76897_76904dup, NG_034012.1:g.76904_76905insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_034012.1:g.76904_76905insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149143008819.

rs1491430088 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->CAAAAAAAAAAAAAAAAAAA
Chromosome:: no mapping
Canonical SPDI:

Select item 149141136520.

rs1491411365 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 6:89809993 (GRCh38)
6:90519712 (GRCh37)
Canonical SPDI:: NC_000006.12:89809992:TA:
Gene:: MDN1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00076/9 (ALFA)
HGVS:: NC_000006.12:g.89809993_89809994del, NC_000006.11:g.90519712_90519713del, NG_034012.1:g.14801_14802del, NW_017363815.1:g.5338_5339del

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