SNP Links for Gene (Select 101409254) - SNP

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Select item 14914989841.

rs1491498984 has merged into rs71205096 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 8:12803842 (GRCh38)
8:12661351 (GRCh37)
Canonical SPDI:: NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.3/12 (GENOME_DK)
TTTTTT=0.4399/2203 (1000Genomes)
HGVS:: NC_000008.11:g.12803842_12803861del, NC_000008.11:g.12803843_12803861del, NC_000008.11:g.12803844_12803861del, NC_000008.11:g.12803845_12803861del, NC_000008.11:g.12803846_12803861del, NC_000008.11:g.12803847_12803861del, NC_000008.11:g.12803848_12803861del, NC_000008.11:g.12803849_12803861del, NC_000008.11:g.12803850_12803861del, NC_000008.11:g.12803851_12803861del, NC_000008.11:g.12803852_12803861del, NC_000008.11:g.12803853_12803861del, NC_000008.11:g.12803854_12803861del, NC_000008.11:g.12803855_12803861del, NC_000008.11:g.12803856_12803861del, NC_000008.11:g.12803857_12803861del, NC_000008.11:g.12803858_12803861del, NC_000008.11:g.12803859_12803861del, NC_000008.11:g.12803860_12803861del, NC_000008.11:g.12803861del, NC_000008.11:g.12803861dup, NC_000008.11:g.12803860_12803861dup, NC_000008.11:g.12803859_12803861dup, NC_000008.11:g.12803858_12803861dup, NC_000008.11:g.12803857_12803861dup, NC_000008.11:g.12803856_12803861dup, NC_000008.11:g.12803855_12803861dup, NC_000008.11:g.12803854_12803861dup, NC_000008.11:g.12803853_12803861dup, NC_000008.11:g.12803852_12803861dup, NC_000008.11:g.12803851_12803861dup, NC_000008.11:g.12803850_12803861dup, NC_000008.11:g.12803848_12803861dup, NC_000008.11:g.12803846_12803861dup, NC_000008.11:g.12803845_12803861dup, NC_000008.11:g.12803844_12803861dup, NC_000008.11:g.12803843_12803861dup, NC_000008.11:g.12803842_12803861dup, NC_000008.11:g.12803841_12803861dup, NC_000008.11:g.12803840_12803861dup, NC_000008.11:g.12803839_12803861dup, NC_000008.10:g.12661351_12661370del, NC_000008.10:g.12661352_12661370del, NC_000008.10:g.12661353_12661370del, NC_000008.10:g.12661354_12661370del, NC_000008.10:g.12661355_12661370del, NC_000008.10:g.12661356_12661370del, NC_000008.10:g.12661357_12661370del, NC_000008.10:g.12661358_12661370del, NC_000008.10:g.12661359_12661370del, NC_000008.10:g.12661360_12661370del, NC_000008.10:g.12661361_12661370del, NC_000008.10:g.12661362_12661370del, NC_000008.10:g.12661363_12661370del, NC_000008.10:g.12661364_12661370del, NC_000008.10:g.12661365_12661370del, NC_000008.10:g.12661366_12661370del, NC_000008.10:g.12661367_12661370del, NC_000008.10:g.12661368_12661370del, NC_000008.10:g.12661369_12661370del, NC_000008.10:g.12661370del, NC_000008.10:g.12661370dup, NC_000008.10:g.12661369_12661370dup, NC_000008.10:g.12661368_12661370dup, NC_000008.10:g.12661367_12661370dup, NC_000008.10:g.12661366_12661370dup, NC_000008.10:g.12661365_12661370dup, NC_000008.10:g.12661364_12661370dup, NC_000008.10:g.12661363_12661370dup, NC_000008.10:g.12661362_12661370dup, NC_000008.10:g.12661361_12661370dup, NC_000008.10:g.12661360_12661370dup, NC_000008.10:g.12661359_12661370dup, NC_000008.10:g.12661357_12661370dup, NC_000008.10:g.12661355_12661370dup, NC_000008.10:g.12661354_12661370dup, NC_000008.10:g.12661353_12661370dup, NC_000008.10:g.12661352_12661370dup, NC_000008.10:g.12661351_12661370dup, NC_000008.10:g.12661350_12661370dup, NC_000008.10:g.12661349_12661370dup, NC_000008.10:g.12661348_12661370dup, NW_018654717.1:g.5999217_5999236del, NW_018654717.1:g.5999218_5999236del, NW_018654717.1:g.5999219_5999236del, NW_018654717.1:g.5999220_5999236del, NW_018654717.1:g.5999221_5999236del, NW_018654717.1:g.5999222_5999236del, NW_018654717.1:g.5999223_5999236del, NW_018654717.1:g.5999224_5999236del, NW_018654717.1:g.5999225_5999236del, NW_018654717.1:g.5999226_5999236del, NW_018654717.1:g.5999227_5999236del, NW_018654717.1:g.5999228_5999236del, NW_018654717.1:g.5999229_5999236del, NW_018654717.1:g.5999230_5999236del, NW_018654717.1:g.5999231_5999236del, NW_018654717.1:g.5999232_5999236del, NW_018654717.1:g.5999233_5999236del, NW_018654717.1:g.5999234_5999236del, NW_018654717.1:g.5999235_5999236del, NW_018654717.1:g.5999236del, NW_018654717.1:g.5999236dup, NW_018654717.1:g.5999235_5999236dup, NW_018654717.1:g.5999234_5999236dup, NW_018654717.1:g.5999233_5999236dup, NW_018654717.1:g.5999232_5999236dup, NW_018654717.1:g.5999231_5999236dup, NW_018654717.1:g.5999230_5999236dup, NW_018654717.1:g.5999229_5999236dup, NW_018654717.1:g.5999228_5999236dup, NW_018654717.1:g.5999227_5999236dup, NW_018654717.1:g.5999226_5999236dup, NW_018654717.1:g.5999225_5999236dup, NW_018654717.1:g.5999223_5999236dup, NW_018654717.1:g.5999221_5999236dup, NW_018654717.1:g.5999220_5999236dup, NW_018654717.1:g.5999219_5999236dup, NW_018654717.1:g.5999218_5999236dup, NW_018654717.1:g.5999217_5999236dup, NW_018654717.1:g.5999216_5999236dup, NW_018654717.1:g.5999215_5999236dup, NW_018654717.1:g.5999214_5999236dup

Select item 14914760392.

rs1491476039 has merged into rs143065417 [Homo sapiens]

Variant type:: DELINS
Alleles:: CC>-,C,CCC,CCCC [Show Flanks]
Chromosome:: 8:12794044 (GRCh38)
8:12651553 (GRCh37)
Canonical SPDI:: NC_000008.11:12794036:CCCCCCCCC:CCCCCCC,NC_000008.11:12794036:CCCCCCCCC:CCCCCCCC,NC_000008.11:12794036:CCCCCCCCC:CCCCCCCCCC,NC_000008.11:12794036:CCCCCCCCC:CCCCCCCCCCC
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCCCCCCCCCC=0./0 (ALFA)
-=0.225/9 (GENOME_DK)
-=0.283083/1091 (ALSPAC)
-=0.287487/1066 (TWINSUK)
-=0.29606/78364 (TOPMED)
-=0.332728/1466 (Estonian)
HGVS:: NC_000008.11:g.12794044_12794045del, NC_000008.11:g.12794045del, NC_000008.11:g.12794045dup, NC_000008.11:g.12794044_12794045dup, NC_000008.10:g.12651553_12651554del, NC_000008.10:g.12651554del, NC_000008.10:g.12651554dup, NC_000008.10:g.12651553_12651554dup, NW_018654717.1:g.5989411_5989412del, NW_018654717.1:g.5989412del, NW_018654717.1:g.5989412dup, NW_018654717.1:g.5989411_5989412dup

Select item 14913140033.

rs1491314003 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 8:12801013 (GRCh38)
8:12658522 (GRCh37)
Canonical SPDI:: NC_000008.11:12801012:CA:
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00101/12 (ALFA)
-=0.00095/26 (TOMMO)
HGVS:: NC_000008.11:g.12801013_12801014del, NC_000008.10:g.12658522_12658523del, NW_018654717.1:g.5996384_5996385del

Select item 14911354644.

rs1491135464 has merged into rs1204150253 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 8:12801025 (GRCh38)
8:12658534 (GRCh37)
Canonical SPDI:: NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:12801013:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000008.11:g.12801025_12801038del, NC_000008.11:g.12801026_12801038del, NC_000008.11:g.12801027_12801038del, NC_000008.11:g.12801028_12801038del, NC_000008.11:g.12801029_12801038del, NC_000008.11:g.12801030_12801038del, NC_000008.11:g.12801031_12801038del, NC_000008.11:g.12801032_12801038del, NC_000008.11:g.12801034_12801038del, NC_000008.11:g.12801035_12801038del, NC_000008.11:g.12801036_12801038del, NC_000008.11:g.12801037_12801038del, NC_000008.11:g.12801038del, NC_000008.11:g.12801038dup, NC_000008.11:g.12801037_12801038dup, NC_000008.11:g.12801036_12801038dup, NC_000008.11:g.12801035_12801038dup, NC_000008.11:g.12801034_12801038dup, NC_000008.11:g.12801033_12801038dup, NC_000008.11:g.12801032_12801038dup, NC_000008.11:g.12801031_12801038dup, NC_000008.11:g.12801024_12801038dup, NC_000008.11:g.12801038_12801039insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000008.10:g.12658534_12658547del, NC_000008.10:g.12658535_12658547del, NC_000008.10:g.12658536_12658547del, NC_000008.10:g.12658537_12658547del, NC_000008.10:g.12658538_12658547del, NC_000008.10:g.12658539_12658547del, NC_000008.10:g.12658540_12658547del, NC_000008.10:g.12658541_12658547del, NC_000008.10:g.12658543_12658547del, NC_000008.10:g.12658544_12658547del, NC_000008.10:g.12658545_12658547del, NC_000008.10:g.12658546_12658547del, NC_000008.10:g.12658547del, NC_000008.10:g.12658547dup, NC_000008.10:g.12658546_12658547dup, NC_000008.10:g.12658545_12658547dup, NC_000008.10:g.12658544_12658547dup, NC_000008.10:g.12658543_12658547dup, NC_000008.10:g.12658542_12658547dup, NC_000008.10:g.12658541_12658547dup, NC_000008.10:g.12658540_12658547dup, NC_000008.10:g.12658533_12658547dup, NC_000008.10:g.12658547_12658548insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NW_018654717.1:g.5996396_5996409del, NW_018654717.1:g.5996397_5996409del, NW_018654717.1:g.5996398_5996409del, NW_018654717.1:g.5996399_5996409del, NW_018654717.1:g.5996400_5996409del, NW_018654717.1:g.5996401_5996409del, NW_018654717.1:g.5996402_5996409del, NW_018654717.1:g.5996403_5996409del, NW_018654717.1:g.5996405_5996409del, NW_018654717.1:g.5996406_5996409del, NW_018654717.1:g.5996407_5996409del, NW_018654717.1:g.5996408_5996409del, NW_018654717.1:g.5996409del, NW_018654717.1:g.5996409dup, NW_018654717.1:g.5996408_5996409dup, NW_018654717.1:g.5996407_5996409dup, NW_018654717.1:g.5996406_5996409dup, NW_018654717.1:g.5996405_5996409dup, NW_018654717.1:g.5996404_5996409dup, NW_018654717.1:g.5996403_5996409dup, NW_018654717.1:g.5996402_5996409dup, NW_018654717.1:g.5996395_5996409dup, NW_018654717.1:g.5996409_5996410insAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14910950235.

rs1491095023 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AATTTTT [Show Flanks]
Chromosome:: 8:12803829 (GRCh38)
8:12661339 (GRCh37)
Canonical SPDI:: NC_000008.11:12803829:TTTTT:TTTTTAATTTTT
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTTTAATTTTT=0./0 (ALFA)
TTTTTAA=0.00004/2 (GnomAD)
HGVS:: NC_000008.11:g.12803830_12803834T[5]AATTTTT[1], NC_000008.10:g.12661339_12661343T[5]AATTTTT[1], NW_018654717.1:g.5999205_5999209T[5]AATTTTT[1]

Select item 14910578526.

rs1491057852 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 8:12795855 (GRCh38)
8:12653364 (GRCh37)
Canonical SPDI:: NC_000008.11:12795853:ATA:A
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000036/5 (GnomAD)
-=0.000045/12 (TOPMED)
-=0.000106/2 (TOMMO)
-=0.000156/1 (1000Genomes)
HGVS:: NC_000008.11:g.12795855_12795856del, NC_000008.10:g.12653364_12653365del, NW_018654717.1:g.5991226_5991227del

Select item 14909558557.

rs1490955855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:12816028 (GRCh38)
8:12673537 (GRCh37)
Canonical SPDI:: NC_000008.11:12816027:A:G
Gene:: LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
HGVS:: NC_000008.11:g.12816028A>G, NC_000008.10:g.12673537A>G, NW_018654717.1:g.6011404A>G

Select item 14908824338.

rs1490882433 has merged into rs71205096 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 8:12803842 (GRCh38)
8:12661351 (GRCh37)
Canonical SPDI:: NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:12803828:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.3/12 (GENOME_DK)
TTTTTT=0.4399/2203 (1000Genomes)
HGVS:: NC_000008.11:g.12803842_12803861del, NC_000008.11:g.12803843_12803861del, NC_000008.11:g.12803844_12803861del, NC_000008.11:g.12803845_12803861del, NC_000008.11:g.12803846_12803861del, NC_000008.11:g.12803847_12803861del, NC_000008.11:g.12803848_12803861del, NC_000008.11:g.12803849_12803861del, NC_000008.11:g.12803850_12803861del, NC_000008.11:g.12803851_12803861del, NC_000008.11:g.12803852_12803861del, NC_000008.11:g.12803853_12803861del, NC_000008.11:g.12803854_12803861del, NC_000008.11:g.12803855_12803861del, NC_000008.11:g.12803856_12803861del, NC_000008.11:g.12803857_12803861del, NC_000008.11:g.12803858_12803861del, NC_000008.11:g.12803859_12803861del, NC_000008.11:g.12803860_12803861del, NC_000008.11:g.12803861del, NC_000008.11:g.12803861dup, NC_000008.11:g.12803860_12803861dup, NC_000008.11:g.12803859_12803861dup, NC_000008.11:g.12803858_12803861dup, NC_000008.11:g.12803857_12803861dup, NC_000008.11:g.12803856_12803861dup, NC_000008.11:g.12803855_12803861dup, NC_000008.11:g.12803854_12803861dup, NC_000008.11:g.12803853_12803861dup, NC_000008.11:g.12803852_12803861dup, NC_000008.11:g.12803851_12803861dup, NC_000008.11:g.12803850_12803861dup, NC_000008.11:g.12803848_12803861dup, NC_000008.11:g.12803846_12803861dup, NC_000008.11:g.12803845_12803861dup, NC_000008.11:g.12803844_12803861dup, NC_000008.11:g.12803843_12803861dup, NC_000008.11:g.12803842_12803861dup, NC_000008.11:g.12803841_12803861dup, NC_000008.11:g.12803840_12803861dup, NC_000008.11:g.12803839_12803861dup, NC_000008.10:g.12661351_12661370del, NC_000008.10:g.12661352_12661370del, NC_000008.10:g.12661353_12661370del, NC_000008.10:g.12661354_12661370del, NC_000008.10:g.12661355_12661370del, NC_000008.10:g.12661356_12661370del, NC_000008.10:g.12661357_12661370del, NC_000008.10:g.12661358_12661370del, NC_000008.10:g.12661359_12661370del, NC_000008.10:g.12661360_12661370del, NC_000008.10:g.12661361_12661370del, NC_000008.10:g.12661362_12661370del, NC_000008.10:g.12661363_12661370del, NC_000008.10:g.12661364_12661370del, NC_000008.10:g.12661365_12661370del, NC_000008.10:g.12661366_12661370del, NC_000008.10:g.12661367_12661370del, NC_000008.10:g.12661368_12661370del, NC_000008.10:g.12661369_12661370del, NC_000008.10:g.12661370del, NC_000008.10:g.12661370dup, NC_000008.10:g.12661369_12661370dup, NC_000008.10:g.12661368_12661370dup, NC_000008.10:g.12661367_12661370dup, NC_000008.10:g.12661366_12661370dup, NC_000008.10:g.12661365_12661370dup, NC_000008.10:g.12661364_12661370dup, NC_000008.10:g.12661363_12661370dup, NC_000008.10:g.12661362_12661370dup, NC_000008.10:g.12661361_12661370dup, NC_000008.10:g.12661360_12661370dup, NC_000008.10:g.12661359_12661370dup, NC_000008.10:g.12661357_12661370dup, NC_000008.10:g.12661355_12661370dup, NC_000008.10:g.12661354_12661370dup, NC_000008.10:g.12661353_12661370dup, NC_000008.10:g.12661352_12661370dup, NC_000008.10:g.12661351_12661370dup, NC_000008.10:g.12661350_12661370dup, NC_000008.10:g.12661349_12661370dup, NC_000008.10:g.12661348_12661370dup, NW_018654717.1:g.5999217_5999236del, NW_018654717.1:g.5999218_5999236del, NW_018654717.1:g.5999219_5999236del, NW_018654717.1:g.5999220_5999236del, NW_018654717.1:g.5999221_5999236del, NW_018654717.1:g.5999222_5999236del, NW_018654717.1:g.5999223_5999236del, NW_018654717.1:g.5999224_5999236del, NW_018654717.1:g.5999225_5999236del, NW_018654717.1:g.5999226_5999236del, NW_018654717.1:g.5999227_5999236del, NW_018654717.1:g.5999228_5999236del, NW_018654717.1:g.5999229_5999236del, NW_018654717.1:g.5999230_5999236del, NW_018654717.1:g.5999231_5999236del, NW_018654717.1:g.5999232_5999236del, NW_018654717.1:g.5999233_5999236del, NW_018654717.1:g.5999234_5999236del, NW_018654717.1:g.5999235_5999236del, NW_018654717.1:g.5999236del, NW_018654717.1:g.5999236dup, NW_018654717.1:g.5999235_5999236dup, NW_018654717.1:g.5999234_5999236dup, NW_018654717.1:g.5999233_5999236dup, NW_018654717.1:g.5999232_5999236dup, NW_018654717.1:g.5999231_5999236dup, NW_018654717.1:g.5999230_5999236dup, NW_018654717.1:g.5999229_5999236dup, NW_018654717.1:g.5999228_5999236dup, NW_018654717.1:g.5999227_5999236dup, NW_018654717.1:g.5999226_5999236dup, NW_018654717.1:g.5999225_5999236dup, NW_018654717.1:g.5999223_5999236dup, NW_018654717.1:g.5999221_5999236dup, NW_018654717.1:g.5999220_5999236dup, NW_018654717.1:g.5999219_5999236dup, NW_018654717.1:g.5999218_5999236dup, NW_018654717.1:g.5999217_5999236dup, NW_018654717.1:g.5999216_5999236dup, NW_018654717.1:g.5999215_5999236dup, NW_018654717.1:g.5999214_5999236dup

Select item 14908332029.

rs1490833202 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:12798817 (GRCh38)
8:12656326 (GRCh37)
Canonical SPDI:: NC_000008.11:12798816:T:A
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.12798817T>A, NC_000008.10:g.12656326T>A, NW_018654717.1:g.5994188T>A

Select item 149058313910.

rs1490583139 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:12818410 (GRCh38)
8:12675919 (GRCh37)
Canonical SPDI:: NC_000008.11:12818409:G:A,NC_000008.11:12818409:G:T
Gene:: LINC00681 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.12818410G>A, NC_000008.11:g.12818410G>T, NC_000008.10:g.12675919G>A, NC_000008.10:g.12675919G>T, NW_018654717.1:g.6013786G>A, NW_018654717.1:g.6013786G>T

Select item 149050760211.

rs1490507602 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 8:12813343 (GRCh38)
8:12670852 (GRCh37)
Canonical SPDI:: NC_000008.11:12813342:C:A,NC_000008.11:12813342:C:G,NC_000008.11:12813342:C:T
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000008.11:g.12813343C>A, NC_000008.11:g.12813343C>G, NC_000008.11:g.12813343C>T, NC_000008.10:g.12670852C>A, NC_000008.10:g.12670852C>G, NC_000008.10:g.12670852C>T, NW_018654717.1:g.6008716C>A, NW_018654717.1:g.6008716C>G, NW_018654717.1:g.6008716C>T

Select item 149029230112.

rs1490292301 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:12797741 (GRCh38)
8:12655250 (GRCh37)
Canonical SPDI:: NC_000008.11:12797740:A:G
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.12797741A>G, NC_000008.10:g.12655250A>G, NW_018654717.1:g.5993112A>G

Select item 149025382213.

rs1490253822 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:12817758 (GRCh38)
8:12675267 (GRCh37)
Canonical SPDI:: NC_000008.11:12817757:G:A
Gene:: LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.12817758G>A, NC_000008.10:g.12675267G>A, NW_018654717.1:g.6013134G>A

Select item 149022877114.

rs1490228771 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:12818478 (GRCh38)
8:12675987 (GRCh37)
Canonical SPDI:: NC_000008.11:12818477:C:G
Gene:: LINC00681 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.12818478C>G, NC_000008.10:g.12675987C>G, NW_018654717.1:g.6013854C>G

Select item 149014193515.

rs1490141935 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:12816754 (GRCh38)
8:12674263 (GRCh37)
Canonical SPDI:: NC_000008.11:12816753:A:G
Gene:: LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000008.11:g.12816754A>G, NC_000008.10:g.12674263A>G, NW_018654717.1:g.6012130A>G

Select item 149012481716.

rs1490124817 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:12812817 (GRCh38)
8:12670326 (GRCh37)
Canonical SPDI:: NC_000008.11:12812816:G:C
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.12812817G>C, NC_000008.10:g.12670326G>C, NW_018654717.1:g.6008190G>C

Select item 148997843617.

rs1489978436 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:12817464 (GRCh38)
8:12674973 (GRCh37)
Canonical SPDI:: NC_000008.11:12817463:A:T
Gene:: LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.12817464A>T, NC_000008.10:g.12674973A>T, NW_018654717.1:g.6012840A>T

Select item 148986758518.

rs1489867585 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 8:12794677 (GRCh38)
8:12652186 (GRCh37)
Canonical SPDI:: NC_000008.11:12794676:T:C,NC_000008.11:12794676:T:G
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.12794677T>C, NC_000008.11:g.12794677T>G, NC_000008.10:g.12652186T>C, NC_000008.10:g.12652186T>G, NW_018654717.1:g.5990044T>C, NW_018654717.1:g.5990044T>G

Select item 148983368419.

rs1489833684 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 8:12793193 (GRCh38)
8:12650702 (GRCh37)
Canonical SPDI:: NC_000008.11:12793192:T:A,NC_000008.11:12793192:T:C
Gene:: LINC03019 (Varview), LINC00681 (Varview)
Functional Consequence:: 2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.12793193T>A, NC_000008.11:g.12793193T>C, NC_000008.10:g.12650702T>A, NC_000008.10:g.12650702T>C, NW_018654717.1:g.5988560T>A, NW_018654717.1:g.5988560T>C

Select item 148964668320.

rs1489646683 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:12817615 (GRCh38)
8:12675124 (GRCh37)
Canonical SPDI:: NC_000008.11:12817614:G:A
Gene:: LINC00681 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.12817615G>A, NC_000008.10:g.12675124G>A, NW_018654717.1:g.6012991G>A

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