SNP Links for Gene (Select 102723617) - SNP

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Select item 14913913841.

rs1491391384 has merged into rs35955765 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:35597309 (GRCh38)
19:36088211 (GRCh37)
Canonical SPDI:: NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:35597295:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC01766 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.1/4 (GENOME_DK)
HGVS:: NC_000019.10:g.35597309_35597319del, NC_000019.10:g.35597311_35597319del, NC_000019.10:g.35597312_35597319del, NC_000019.10:g.35597313_35597319del, NC_000019.10:g.35597315_35597319del, NC_000019.10:g.35597316_35597319del, NC_000019.10:g.35597317_35597319del, NC_000019.10:g.35597318_35597319del, NC_000019.10:g.35597319del, NC_000019.10:g.35597319dup, NC_000019.10:g.35597318_35597319dup, NC_000019.10:g.35597317_35597319dup, NC_000019.10:g.35597316_35597319dup, NC_000019.10:g.35597314_35597319dup, NC_000019.10:g.35597313_35597319dup, NC_000019.10:g.35597304_35597319dup, NC_000019.10:g.35597298_35597319dup, NC_000019.10:g.35597297_35597319dup, NC_000019.10:g.35597319_35597320insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.36088211_36088221del, NC_000019.9:g.36088213_36088221del, NC_000019.9:g.36088214_36088221del, NC_000019.9:g.36088215_36088221del, NC_000019.9:g.36088217_36088221del, NC_000019.9:g.36088218_36088221del, NC_000019.9:g.36088219_36088221del, NC_000019.9:g.36088220_36088221del, NC_000019.9:g.36088221del, NC_000019.9:g.36088221dup, NC_000019.9:g.36088220_36088221dup, NC_000019.9:g.36088219_36088221dup, NC_000019.9:g.36088218_36088221dup, NC_000019.9:g.36088216_36088221dup, NC_000019.9:g.36088215_36088221dup, NC_000019.9:g.36088206_36088221dup, NC_000019.9:g.36088200_36088221dup, NC_000019.9:g.36088199_36088221dup, NC_000019.9:g.36088221_36088222insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14912445782.

rs1491244578 has merged into rs60709115 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:35597776 (GRCh38)
19:36088678 (GRCh37)
Canonical SPDI:: NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC01766 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.35597776_35597793del, NC_000019.10:g.35597777_35597793del, NC_000019.10:g.35597778_35597793del, NC_000019.10:g.35597779_35597793del, NC_000019.10:g.35597780_35597793del, NC_000019.10:g.35597781_35597793del, NC_000019.10:g.35597782_35597793del, NC_000019.10:g.35597783_35597793del, NC_000019.10:g.35597784_35597793del, NC_000019.10:g.35597785_35597793del, NC_000019.10:g.35597786_35597793del, NC_000019.10:g.35597787_35597793del, NC_000019.10:g.35597788_35597793del, NC_000019.10:g.35597789_35597793del, NC_000019.10:g.35597790_35597793del, NC_000019.10:g.35597791_35597793del, NC_000019.10:g.35597792_35597793del, NC_000019.10:g.35597793del, NC_000019.10:g.35597793dup, NC_000019.10:g.35597792_35597793dup, NC_000019.10:g.35597791_35597793dup, NC_000019.10:g.35597790_35597793dup, NC_000019.10:g.35597787_35597793dup, NC_000019.10:g.35597786_35597793dup, NC_000019.9:g.36088678_36088695del, NC_000019.9:g.36088679_36088695del, NC_000019.9:g.36088680_36088695del, NC_000019.9:g.36088681_36088695del, NC_000019.9:g.36088682_36088695del, NC_000019.9:g.36088683_36088695del, NC_000019.9:g.36088684_36088695del, NC_000019.9:g.36088685_36088695del, NC_000019.9:g.36088686_36088695del, NC_000019.9:g.36088687_36088695del, NC_000019.9:g.36088688_36088695del, NC_000019.9:g.36088689_36088695del, NC_000019.9:g.36088690_36088695del, NC_000019.9:g.36088691_36088695del, NC_000019.9:g.36088692_36088695del, NC_000019.9:g.36088693_36088695del, NC_000019.9:g.36088694_36088695del, NC_000019.9:g.36088695del, NC_000019.9:g.36088695dup, NC_000019.9:g.36088694_36088695dup, NC_000019.9:g.36088693_36088695dup, NC_000019.9:g.36088692_36088695dup, NC_000019.9:g.36088689_36088695dup, NC_000019.9:g.36088688_36088695dup

Select item 14911850033.

rs1491185003 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 19:35597766 (GRCh38)
19:36088668 (GRCh37)
Canonical SPDI:: NC_000019.10:35597765:GA:
Gene:: LINC01766 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00025/3 (ALFA)
-=0.00101/16 (TOMMO)
HGVS:: NC_000019.10:g.35597766_35597767del, NC_000019.9:g.36088668_36088669del

Select item 14911562834.

rs1491156283 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 19:35597295 (GRCh38)
19:36088197 (GRCh37)
Canonical SPDI:: NC_000019.10:35597294:AT:
Gene:: LINC01766 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00047/3 (1000Genomes)
HGVS:: NC_000019.10:g.35597295_35597296del, NC_000019.9:g.36088197_36088198del

Select item 14904241035.

rs1490424103 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:35596157 (GRCh38)
19:36087059 (GRCh37)
Canonical SPDI:: NC_000019.10:35596156:G:A,NC_000019.10:35596156:G:C
Gene:: LINC01766 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.35596157G>A, NC_000019.10:g.35596157G>C, NC_000019.9:g.36087059G>A, NC_000019.9:g.36087059G>C

Select item 14897006156.

rs1489700615 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:35601497 (GRCh38)
19:36092399 (GRCh37)
Canonical SPDI:: NC_000019.10:35601496:A:G
Gene:: LINC01766 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.35601497A>G, NC_000019.9:g.36092399A>G, NR_110750.1:n.370A>G

Select item 14891055577.

rs1489105557 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:35597022 (GRCh38)
19:36087924 (GRCh37)
Canonical SPDI:: NC_000019.10:35597021:C:T
Gene:: LINC01766 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.35597022C>T, NC_000019.9:g.36087924C>T

Select item 14875645378.

rs1487564537 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:35598632 (GRCh38)
19:36089534 (GRCh37)
Canonical SPDI:: NC_000019.10:35598631:C:A,NC_000019.10:35598631:C:T
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000008/1 (GnomAD)
HGVS:: NC_000019.10:g.35598632C>A, NC_000019.10:g.35598632C>T, NC_000019.9:g.36089534C>A, NC_000019.9:g.36089534C>T

Select item 14875022539.

rs1487502253 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:35598757 (GRCh38)
19:36089659 (GRCh37)
Canonical SPDI:: NC_000019.10:35598756:G:T
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.35598757G>T, NC_000019.9:g.36089659G>T

Select item 148593596110.

rs1485935961 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:35599267 (GRCh38)
19:36090169 (GRCh37)
Canonical SPDI:: NC_000019.10:35599266:G:A
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000061/1 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000022/3 (GnomAD)
HGVS:: NC_000019.10:g.35599267G>A, NC_000019.9:g.36090169G>A

Select item 148577039811.

rs1485770398 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:35599687 (GRCh38)
19:36090589 (GRCh37)
Canonical SPDI:: NC_000019.10:35599686:A:G
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000019.10:g.35599687A>G, NC_000019.9:g.36090589A>G

Select item 148560725012.

rs1485607250 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:35599619 (GRCh38)
19:36090521 (GRCh37)
Canonical SPDI:: NC_000019.10:35599618:C:A
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.35599619C>A, NC_000019.9:g.36090521C>A

Select item 148550455913.

rs1485504559 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:35599347 (GRCh38)
19:36090249 (GRCh37)
Canonical SPDI:: NC_000019.10:35599346:A:C
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.35599347A>C, NC_000019.9:g.36090249A>C

Select item 148525017914.

rs1485250179 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:35600331 (GRCh38)
19:36091233 (GRCh37)
Canonical SPDI:: NC_000019.10:35600330:A:G
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000019.10:g.35600331A>G, NC_000019.9:g.36091233A>G

Select item 148487520515.

rs1484875205 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 19:35596100 (GRCh38)
19:36087002 (GRCh37)
Canonical SPDI:: NC_000019.10:35596099:G:A,NC_000019.10:35596099:G:C
Gene:: LINC01766 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000019.10:g.35596100G>A, NC_000019.10:g.35596100G>C, NC_000019.9:g.36087002G>A, NC_000019.9:g.36087002G>C

Select item 148449480816.

rs1484494808 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:35597890 (GRCh38)
19:36088792 (GRCh37)
Canonical SPDI:: NC_000019.10:35597889:C:G,NC_000019.10:35597889:C:T
Gene:: LINC01766 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000142/2 (TOMMO)
HGVS:: NC_000019.10:g.35597890C>G, NC_000019.10:g.35597890C>T, NC_000019.9:g.36088792C>G, NC_000019.9:g.36088792C>T

Select item 148448147917.

rs1484481479 [Homo sapiens]

Variant type:: DELINS
Alleles:: GCCTGTAATCCCAGCAC>- [Show Flanks]
Chromosome:: 19:35600158 (GRCh38)
19:36091060 (GRCh37)
Canonical SPDI:: NC_000019.10:35600154:CACGCCTGTAATCCCAGCAC:CAC
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CAC=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.35600158_35600174del, NC_000019.9:g.36091060_36091076del

Select item 148361153818.

rs1483611538 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:35600525 (GRCh38)
19:36091427 (GRCh37)
Canonical SPDI:: NC_000019.10:35600524:A:G
Gene:: LINC01766 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.35600525A>G, NC_000019.9:g.36091427A>G

Select item 148284600919.

rs1482846009 has merged into rs60709115 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 19:35597776 (GRCh38)
19:36088678 (GRCh37)
Canonical SPDI:: NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:35597766:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC01766 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000019.10:g.35597776_35597793del, NC_000019.10:g.35597777_35597793del, NC_000019.10:g.35597778_35597793del, NC_000019.10:g.35597779_35597793del, NC_000019.10:g.35597780_35597793del, NC_000019.10:g.35597781_35597793del, NC_000019.10:g.35597782_35597793del, NC_000019.10:g.35597783_35597793del, NC_000019.10:g.35597784_35597793del, NC_000019.10:g.35597785_35597793del, NC_000019.10:g.35597786_35597793del, NC_000019.10:g.35597787_35597793del, NC_000019.10:g.35597788_35597793del, NC_000019.10:g.35597789_35597793del, NC_000019.10:g.35597790_35597793del, NC_000019.10:g.35597791_35597793del, NC_000019.10:g.35597792_35597793del, NC_000019.10:g.35597793del, NC_000019.10:g.35597793dup, NC_000019.10:g.35597792_35597793dup, NC_000019.10:g.35597791_35597793dup, NC_000019.10:g.35597790_35597793dup, NC_000019.10:g.35597787_35597793dup, NC_000019.10:g.35597786_35597793dup, NC_000019.9:g.36088678_36088695del, NC_000019.9:g.36088679_36088695del, NC_000019.9:g.36088680_36088695del, NC_000019.9:g.36088681_36088695del, NC_000019.9:g.36088682_36088695del, NC_000019.9:g.36088683_36088695del, NC_000019.9:g.36088684_36088695del, NC_000019.9:g.36088685_36088695del, NC_000019.9:g.36088686_36088695del, NC_000019.9:g.36088687_36088695del, NC_000019.9:g.36088688_36088695del, NC_000019.9:g.36088689_36088695del, NC_000019.9:g.36088690_36088695del, NC_000019.9:g.36088691_36088695del, NC_000019.9:g.36088692_36088695del, NC_000019.9:g.36088693_36088695del, NC_000019.9:g.36088694_36088695del, NC_000019.9:g.36088695del, NC_000019.9:g.36088695dup, NC_000019.9:g.36088694_36088695dup, NC_000019.9:g.36088693_36088695dup, NC_000019.9:g.36088692_36088695dup, NC_000019.9:g.36088689_36088695dup, NC_000019.9:g.36088688_36088695dup

Select item 148204395920.

rs1482043959 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:35601966 (GRCh38)
19:36092868 (GRCh37)
Canonical SPDI:: NC_000019.10:35601965:C:G
Gene:: LINC01766 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
G=0.000779/13 (TOMMO)
HGVS:: NC_000019.10:g.35601966C>G, NC_000019.9:g.36092868C>G

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