SNP Links for Gene (Select 434) - SNP

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Select item 14915836921.

rs1491583692 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 20:34257061 (GRCh38)
20:32844868 (GRCh37)
Canonical SPDI:: NC_000020.11:34257061::C
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000076/8 (GnomAD)
HGVS:: NC_000020.11:g.34257061_34257062insC, NC_000020.10:g.32844867_32844868insC, NG_011439.1:g.1697_1698insC

Select item 14915764052.

rs1491576405 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 20:34220954 (GRCh38)
20:32808761 (GRCh37)
Canonical SPDI:: NC_000020.11:34220954:T:TCT
Gene:: ASIP (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TCT=0./0 (ALFA)
HGVS:: NC_000020.11:g.34220955_34220956insCT, NC_000020.10:g.32808761_32808762insCT

Select item 14915482683.

rs1491548268 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 20:34194524 (GRCh38)
20:32782331 (GRCh37)
Canonical SPDI:: NC_000020.11:34194524::A
Gene:: ASIP (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000020.11:g.34194524_34194525insA, NC_000020.10:g.32782330_32782331insA

Select item 14915207464.

rs1491520746 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 20:34258769 (GRCh38)
20:32846575 (GRCh37)
Canonical SPDI:: NC_000020.11:34258768:AA:
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00008/1 (ALFA)
-=0.00003/3 (GnomAD)
-=0.00004/1 (TOMMO)
HGVS:: NC_000020.11:g.34258769_34258770del, NC_000020.10:g.32846575_32846576del, NG_011439.1:g.3405_3406del

Select item 14914742175.

rs1491474217 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAAAG [Show Flanks]
Chromosome:: 20:34235820 (GRCh38)
20:32823627 (GRCh37)
Canonical SPDI:: NC_000020.11:34235820:GAAAG:GAAAGGAAAG
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAAAGGAAAG=0./0 (ALFA)
GAAAG=0.00003/2 (GnomAD)
HGVS:: NC_000020.11:g.34235821_34235825dup, NC_000020.10:g.32823627_32823631dup

Select item 14914621466.

rs1491462146 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 20:34201020 (GRCh38)
20:32788826 (GRCh37)
Canonical SPDI:: NC_000020.11:34201018:TCT:T
Gene:: ASIP (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000020.11:g.34201020_34201021del, NC_000020.10:g.32788826_32788827del

Select item 14914467907.

rs1491446790 has merged into rs1354827327 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATA>-,TA,TATATA [Show Flanks]
Chromosome:: 20:34258775 (GRCh38)
20:32846581 (GRCh37)
Canonical SPDI:: NC_000020.11:34258769:ATATATATA:ATATA,NC_000020.11:34258769:ATATATATA:ATATATA,NC_000020.11:34258769:ATATATATA:ATATATATATA
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000595/1 (Korea1K)
-=0.001093/7 (1000Genomes)
-=0.001431/24 (TOMMO)
HGVS:: NC_000020.11:g.34258771TA[2], NC_000020.11:g.34258771TA[3], NC_000020.11:g.34258771TA[5], NC_000020.10:g.32846577TA[2], NC_000020.10:g.32846577TA[3], NC_000020.10:g.32846577TA[5], NG_011439.1:g.3407TA[2], NG_011439.1:g.3407TA[3], NG_011439.1:g.3407TA[5]

Select item 14914299068.

rs1491429906 has merged into rs772655085 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATATA>-,TA,TATA,TATATA,TATATATAATATATATATATATATATATATATATA,TATATATATA,TATATATATACACTATATATATATATATATATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATACATACTATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATTATATATATATATATATATA,TATATATATCTATATATATATATATATATATATATA [Show Flanks]
Chromosome:: 20:34258684 (GRCh38)
20:32846490 (GRCh37)
Canonical SPDI:: NC_000020.11:34258674:ATATATATATATATATA:ATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATAATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATACACTATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATACATACTATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATATATATATTATATATATATATATATATA,NC_000020.11:34258674:ATATATATATATATATA:ATATATATATATATATATCTATATATATATATATATATATATATA
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATA=0./0 (ALFA)
ATATATATATATATATATATATAT=0.175/7 (GENOME_DK)
HGVS:: NC_000020.11:g.34258676TA[4], NC_000020.11:g.34258676TA[5], NC_000020.11:g.34258676TA[6], NC_000020.11:g.34258676TA[7], NC_000020.11:g.34258675_34258691ATATATATATATATATA[2]TA[5], NC_000020.11:g.34258676TA[9], NC_000020.11:g.34258675_34258691AT[9]AC[2]TA[13], NC_000020.11:g.34258676TA[10], NC_000020.11:g.34258676TA[11], NC_000020.11:g.34258676TA[12], NC_000020.11:g.34258676TA[13], NC_000020.11:g.34258676TA[14], NC_000020.11:g.34258676TA[15], NC_000020.11:g.34258676TA[16], NC_000020.11:g.34258676TA[17], NC_000020.11:g.34258676TA[18], NC_000020.11:g.34258676TA[19], NC_000020.11:g.34258675_34258691AT[19]ACATACTATATATATATATATATATATATATATATA[1], NC_000020.11:g.34258676TA[20], NC_000020.11:g.34258676TA[21], NC_000020.11:g.34258676TA[22], NC_000020.11:g.34258676TA[23], NC_000020.11:g.34258676TA[24], NC_000020.11:g.34258676TA[26], NC_000020.11:g.34258676TA[27], NC_000020.11:g.34258675_34258691AT[13]TA[10], NC_000020.11:g.34258675_34258691AT[9]CTATATATATATATATATATATATATA[1], NC_000020.10:g.32846482TA[4], NC_000020.10:g.32846482TA[5], NC_000020.10:g.32846482TA[6], NC_000020.10:g.32846482TA[7], NC_000020.10:g.32846481_32846497ATATATATATATATATA[2]TA[5], NC_000020.10:g.32846482TA[9], NC_000020.10:g.32846481_32846497AT[9]AC[2]TA[13], NC_000020.10:g.32846482TA[10], NC_000020.10:g.32846482TA[11], NC_000020.10:g.32846482TA[12], NC_000020.10:g.32846482TA[13], NC_000020.10:g.32846482TA[14], NC_000020.10:g.32846482TA[15], NC_000020.10:g.32846482TA[16], NC_000020.10:g.32846482TA[17], NC_000020.10:g.32846482TA[18], NC_000020.10:g.32846482TA[19], NC_000020.10:g.32846481_32846497AT[19]ACATACTATATATATATATATATATATATATATATA[1], NC_000020.10:g.32846482TA[20], NC_000020.10:g.32846482TA[21], NC_000020.10:g.32846482TA[22], NC_000020.10:g.32846482TA[23], NC_000020.10:g.32846482TA[24], NC_000020.10:g.32846482TA[26], NC_000020.10:g.32846482TA[27], NC_000020.10:g.32846481_32846497AT[13]TA[10], NC_000020.10:g.32846481_32846497AT[9]CTATATATATATATATATATATATATA[1], NG_011439.1:g.3312TA[4], NG_011439.1:g.3312TA[5], NG_011439.1:g.3312TA[6], NG_011439.1:g.3312TA[7], NG_011439.1:g.3311_3327ATATATATATATATATA[2]TA[5], NG_011439.1:g.3312TA[9], NG_011439.1:g.3311_3327AT[9]AC[2]TA[13], NG_011439.1:g.3312TA[10], NG_011439.1:g.3312TA[11], NG_011439.1:g.3312TA[12], NG_011439.1:g.3312TA[13], NG_011439.1:g.3312TA[14], NG_011439.1:g.3312TA[15], NG_011439.1:g.3312TA[16], NG_011439.1:g.3312TA[17], NG_011439.1:g.3312TA[18], NG_011439.1:g.3312TA[19], NG_011439.1:g.3311_3327AT[19]ACATACTATATATATATATATATATATATATATATA[1], NG_011439.1:g.3312TA[20], NG_011439.1:g.3312TA[21], NG_011439.1:g.3312TA[22], NG_011439.1:g.3312TA[23], NG_011439.1:g.3312TA[24], NG_011439.1:g.3312TA[26], NG_011439.1:g.3312TA[27], NG_011439.1:g.3311_3327AT[13]TA[10], NG_011439.1:g.3311_3327AT[9]CTATATATATATATATATATATATATA[1]

Select item 14913402859.

rs1491340285 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: 20:34197005 (GRCh38)
20:32784811 (GRCh37)
Canonical SPDI:: NC_000020.11:34197004:AAA:AA,NC_000020.11:34197004:AAA:AAAA
Gene:: ASIP (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0./0 (ALFA)
-=0.000015/2 (GnomAD)
-=0.000035/1 (TOMMO)
HGVS:: NC_000020.11:g.34197007del, NC_000020.11:g.34197007dup, NC_000020.10:g.32784813del, NC_000020.10:g.32784813dup

Select item 149133255510.

rs1491332555 has merged into rs58407816 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 20:34191741 (GRCh38)
20:32779547 (GRCh37)
Canonical SPDI:: NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34191730:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ASIP (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000020.11:g.34191741_34191748del, NC_000020.11:g.34191742_34191748del, NC_000020.11:g.34191743_34191748del, NC_000020.11:g.34191744_34191748del, NC_000020.11:g.34191745_34191748del, NC_000020.11:g.34191746_34191748del, NC_000020.11:g.34191747_34191748del, NC_000020.11:g.34191748del, NC_000020.11:g.34191748dup, NC_000020.11:g.34191747_34191748dup, NC_000020.11:g.34191746_34191748dup, NC_000020.11:g.34191745_34191748dup, NC_000020.11:g.34191744_34191748dup, NC_000020.11:g.34191743_34191748dup, NC_000020.11:g.34191742_34191748dup, NC_000020.11:g.34191740_34191748dup, NC_000020.10:g.32779547_32779554del, NC_000020.10:g.32779548_32779554del, NC_000020.10:g.32779549_32779554del, NC_000020.10:g.32779550_32779554del, NC_000020.10:g.32779551_32779554del, NC_000020.10:g.32779552_32779554del, NC_000020.10:g.32779553_32779554del, NC_000020.10:g.32779554del, NC_000020.10:g.32779554dup, NC_000020.10:g.32779553_32779554dup, NC_000020.10:g.32779552_32779554dup, NC_000020.10:g.32779551_32779554dup, NC_000020.10:g.32779550_32779554dup, NC_000020.10:g.32779549_32779554dup, NC_000020.10:g.32779548_32779554dup, NC_000020.10:g.32779546_32779554dup

Select item 149133170511.

rs1491331705 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 20:34235821 (GRCh38)
20:32823627 (GRCh37)
Canonical SPDI:: NC_000020.11:34235819:AGA:A
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.00002/1 (GnomAD)
HGVS:: NC_000020.11:g.34235821_34235822del, NC_000020.10:g.32823627_32823628del

Select item 149131352512.

rs1491313525 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 20:34197004 (GRCh38)
20:32784810 (GRCh37)
Canonical SPDI:: NC_000020.11:34197003:TA:
Gene:: ASIP (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000020.11:g.34197004_34197005del, NC_000020.10:g.32784810_32784811del

Select item 149130024713.

rs1491300247 has merged into rs10661983 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,T,TT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 20:34220963 (GRCh38)
20:32808769 (GRCh37)
Canonical SPDI:: NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34220953:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: ASIP (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000020.11:g.34220963_34220976del, NC_000020.11:g.34220964_34220976del, NC_000020.11:g.34220965_34220976del, NC_000020.11:g.34220968_34220976del, NC_000020.11:g.34220969_34220976del, NC_000020.11:g.34220970_34220976del, NC_000020.11:g.34220971_34220976del, NC_000020.11:g.34220972_34220976del, NC_000020.11:g.34220973_34220976del, NC_000020.11:g.34220974_34220976del, NC_000020.11:g.34220975_34220976del, NC_000020.11:g.34220976del, NC_000020.11:g.34220976dup, NC_000020.11:g.34220975_34220976dup, NC_000020.11:g.34220974_34220976dup, NC_000020.11:g.34220973_34220976dup, NC_000020.11:g.34220971_34220976dup, NC_000020.11:g.34220970_34220976dup, NC_000020.11:g.34220969_34220976dup, NC_000020.11:g.34220968_34220976dup, NC_000020.11:g.34220967_34220976dup, NC_000020.11:g.34220965_34220976dup, NC_000020.11:g.34220964_34220976dup, NC_000020.11:g.34220963_34220976dup, NC_000020.11:g.34220959_34220976dup, NC_000020.10:g.32808769_32808782del, NC_000020.10:g.32808770_32808782del, NC_000020.10:g.32808771_32808782del, NC_000020.10:g.32808774_32808782del, NC_000020.10:g.32808775_32808782del, NC_000020.10:g.32808776_32808782del, NC_000020.10:g.32808777_32808782del, NC_000020.10:g.32808778_32808782del, NC_000020.10:g.32808779_32808782del, NC_000020.10:g.32808780_32808782del, NC_000020.10:g.32808781_32808782del, NC_000020.10:g.32808782del, NC_000020.10:g.32808782dup, NC_000020.10:g.32808781_32808782dup, NC_000020.10:g.32808780_32808782dup, NC_000020.10:g.32808779_32808782dup, NC_000020.10:g.32808777_32808782dup, NC_000020.10:g.32808776_32808782dup, NC_000020.10:g.32808775_32808782dup, NC_000020.10:g.32808774_32808782dup, NC_000020.10:g.32808773_32808782dup, NC_000020.10:g.32808771_32808782dup, NC_000020.10:g.32808770_32808782dup, NC_000020.10:g.32808769_32808782dup, NC_000020.10:g.32808765_32808782dup

Select item 149126931114.

rs1491269311 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTA [Show Flanks]
Chromosome:: 20:34258770 (GRCh38)
20:32846577 (GRCh37)
Canonical SPDI:: NC_000020.11:34258770:TA:TACTA
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TACTA=0.00615/73 (ALFA)
HGVS:: NC_000020.11:g.34258772_34258773insCTA, NC_000020.10:g.32846578_32846579insCTA, NG_011439.1:g.3408_3409insCTA

Select item 149125071915.

rs1491250719 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,GGA,GGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGA,GGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,GGAAGGA,GGAAGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,GGAAGGAAGGA,GGAAGGAAGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,GGAAGGAGGAGGGAGGGAAGAATGA,GGAGGAGGGAGGGAAGAAAGA,GGAGGAGGGAGGGAAGAATGA,GGAGGAGGGAGGGAAGAATGAAGA,GGGA [Show Flanks]
Chromosome:: 20:34235899 (GRCh38)
20:32823706 (GRCh37)
Canonical SPDI:: NC_000020.11:34235899:A:AGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,NC_000020.11:34235899:A:AGGA,NC_000020.11:34235899:A:AGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGA,NC_000020.11:34235899:A:AGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,NC_000020.11:34235899:A:AGGAAGGA,NC_000020.11:34235899:A:AGGAAGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,NC_000020.11:34235899:A:AGGAAGGAAGGA,NC_000020.11:34235899:A:AGGAAGGAAGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA,NC_000020.11:34235899:A:AGGAAGGAGGAGGGAGGGAAGAATGA,NC_000020.11:34235899:A:AGGAGGAGGGAGGGAAGAAAGA,NC_000020.11:34235899:A:AGGAGGAGGGAGGGAAGAATGA,NC_000020.11:34235899:A:AGGAGGAGGGAGGGAAGAATGAAGA,NC_000020.11:34235899:A:AGGGA
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGGA=0./0 (ALFA)
AGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATG=0.01552/9 (NorthernSweden)
HGVS:: NC_000020.11:g.34235900_34235901insGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA, NC_000020.11:g.34235900_34235901insGGA, NC_000020.11:g.34235900_34235901insGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGA, NC_000020.11:g.34235900_34235901insGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA, NC_000020.11:g.34235900_34235901insGGAAGGA, NC_000020.11:g.34235900AGGA[2]AGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA[1], NC_000020.11:g.34235900_34235901insGGAAGGAAGGA, NC_000020.11:g.34235900AGGA[3]AGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA[1], NC_000020.11:g.34235900AGGA[2]GGAG[2]GGAAGAATGA[1], NC_000020.11:g.34235900AGG[3]GAGGGAAGAAAGA[1], NC_000020.11:g.34235900AGG[3]GAGGGAAGAATGA[1], NC_000020.11:g.34235900AGG[3]GAGGGAAGAATGAAGA[1], NC_000020.11:g.34235900_34235901insGGGA, NC_000020.10:g.32823706_32823707insGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA, NC_000020.10:g.32823706_32823707insGGA, NC_000020.10:g.32823706_32823707insGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGA, NC_000020.10:g.32823706_32823707insGGAAGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA, NC_000020.10:g.32823706_32823707insGGAAGGA, NC_000020.10:g.32823706AGGA[2]AGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA[1], NC_000020.10:g.32823706_32823707insGGAAGGAAGGA, NC_000020.10:g.32823706AGGA[3]AGCGGGAGGGAGGGAAGAAGGAAGGAAGGAGGAGGGAGGGAAGAATGA[1], NC_000020.10:g.32823706AGGA[2]GGAG[2]GGAAGAATGA[1], NC_000020.10:g.32823706AGG[3]GAGGGAAGAAAGA[1], NC_000020.10:g.32823706AGG[3]GAGGGAAGAATGA[1], NC_000020.10:g.32823706AGG[3]GAGGGAAGAATGAAGA[1], NC_000020.10:g.32823706_32823707insGGGA

Select item 149123685516.

rs1491236855 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 20:34258709 (GRCh38)
20:32846515 (GRCh37)
Canonical SPDI:: NC_000020.11:34258708:TT:
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00004/3 (GnomAD)
HGVS:: NC_000020.11:g.34258709_34258710del, NC_000020.10:g.32846515_32846516del, NG_011439.1:g.3345_3346del

Select item 149122842317.

rs1491228423 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 20:34245841 (GRCh38)
20:32833647 (GRCh37)
Canonical SPDI:: NC_000020.11:34245840:AA:
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.34245841_34245842del, NC_000020.10:g.32833647_32833648del, NG_021981.2:g.796_797del

Select item 149121811118.

rs1491218111 [Homo sapiens]

Variant type:: DEL
Alleles:: GG>- [Show Flanks]
Chromosome:: 20:34194524 (GRCh38)
20:32782330 (GRCh37)
Canonical SPDI:: NC_000020.11:34194523:GG:
Gene:: ASIP (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00007/1 (ALFA)
HGVS:: NC_000020.11:g.34194524_34194525del, NC_000020.10:g.32782330_32782331del

Select item 149121584219.

rs1491215842 [Homo sapiens]

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

Select item 149119173520.

rs1491191735 has merged into rs56227909 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 20:34257076 (GRCh38)
20:32844882 (GRCh37)
Canonical SPDI:: NC_000020.11:34257070:TTTTTTTTTTTT:TTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:34257070:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: AHCY (Varview), ASIP (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTT=0./0 (ALFA)
-=0.000045/12 (TOPMED)
T=0.353834/1772 (1000Genomes)
HGVS:: NC_000020.11:g.34257076_34257082del, NC_000020.11:g.34257078_34257082del, NC_000020.11:g.34257079_34257082del, NC_000020.11:g.34257080_34257082del, NC_000020.11:g.34257081_34257082del, NC_000020.11:g.34257082del, NC_000020.11:g.34257082dup, NC_000020.11:g.34257081_34257082dup, NC_000020.11:g.34257080_34257082dup, NC_000020.11:g.34257079_34257082dup, NC_000020.11:g.34257078_34257082dup, NC_000020.11:g.34257077_34257082dup, NC_000020.11:g.34257076_34257082dup, NC_000020.11:g.34257075_34257082dup, NC_000020.11:g.34257074_34257082dup, NC_000020.11:g.34257073_34257082dup, NC_000020.11:g.34257072_34257082dup, NC_000020.11:g.34257071_34257082dup, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.11:g.34257082_34257083insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844882_32844888del, NC_000020.10:g.32844884_32844888del, NC_000020.10:g.32844885_32844888del, NC_000020.10:g.32844886_32844888del, NC_000020.10:g.32844887_32844888del, NC_000020.10:g.32844888del, NC_000020.10:g.32844888dup, NC_000020.10:g.32844887_32844888dup, NC_000020.10:g.32844886_32844888dup, NC_000020.10:g.32844885_32844888dup, NC_000020.10:g.32844884_32844888dup, NC_000020.10:g.32844883_32844888dup, NC_000020.10:g.32844882_32844888dup, NC_000020.10:g.32844881_32844888dup, NC_000020.10:g.32844880_32844888dup, NC_000020.10:g.32844879_32844888dup, NC_000020.10:g.32844878_32844888dup, NC_000020.10:g.32844877_32844888dup, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000020.10:g.32844888_32844889insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1712_1718del, NG_011439.1:g.1714_1718del, NG_011439.1:g.1715_1718del, NG_011439.1:g.1716_1718del, NG_011439.1:g.1717_1718del, NG_011439.1:g.1718del, NG_011439.1:g.1718dup, NG_011439.1:g.1717_1718dup, NG_011439.1:g.1716_1718dup, NG_011439.1:g.1715_1718dup, NG_011439.1:g.1714_1718dup, NG_011439.1:g.1713_1718dup, NG_011439.1:g.1712_1718dup, NG_011439.1:g.1711_1718dup, NG_011439.1:g.1710_1718dup, NG_011439.1:g.1709_1718dup, NG_011439.1:g.1708_1718dup, NG_011439.1:g.1707_1718dup, NG_011439.1:g.1718_1719insTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_011439.1:g.1718_1719insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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