SNP Links for Nucleotide (Select 343403818) - SNP

Links from Nucleotide

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Select item 14868338551.

rs1486833855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32391632 (GRCh38)
6:32359409 (GRCh37)
Canonical SPDI:: NC_000006.12:32391631:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
HGVS:: NC_000006.12:g.32391632A>G, NC_000006.11:g.32359409A>G, NG_054759.1:g.22248T>C, NT_113891.3:g.3829732A>G, NT_113891.2:g.3829838A>G, NT_167244.2:g.3723863A>G, NT_167244.1:g.3673779A>G, NT_167248.2:g.3614672A>G, NT_167248.1:g.3620268A>G, NT_167246.2:g.3696625A>G, NT_167246.1:g.3702245A>G, NT_167249.2:g.3707554A>G, NT_167249.1:g.3706852A>G, NT_167247.2:g.3733382A>G, NT_167247.1:g.3738967A>G, NT_167245.2:g.3632723A>G, NT_167245.1:g.3638308A>G, NT_187692.1:g.62329T>C, NR_044996.1:n.264A>G

Select item 14859800072.

rs1485980007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:32390530 (GRCh38)
6:32358307 (GRCh37)
Canonical SPDI:: NC_000006.12:32390529:C:T
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.32390530C>T, NC_000006.11:g.32358307C>T, NT_113891.3:g.3828630C>T, NT_113891.2:g.3828736C>T, NT_167248.2:g.3613570C>T, NT_167248.1:g.3619166C>T, NT_167245.2:g.3631621C>T, NT_167245.1:g.3637206C>T, NT_167249.2:g.3706451C>T, NT_167249.1:g.3705749C>T, NT_167246.2:g.3695522C>T, NT_167246.1:g.3701142C>T, NT_167247.2:g.3732279C>T, NT_167247.1:g.3737864C>T, NT_167244.2:g.3722761C>T, NT_167244.1:g.3672677C>T, NT_187692.1:g.63437G>A, NR_044996.1:n.21C>T

Select item 14859484283.

rs1485948428 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:32391735 (GRCh38)
6:32359512 (GRCh37)
Canonical SPDI:: NC_000006.12:32391734:T:C
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.32391735T>C, NC_000006.11:g.32359512T>C, NG_054759.1:g.22145A>G, NT_113891.3:g.3829835T>C, NT_113891.2:g.3829941T>C, NT_167244.2:g.3723966T>C, NT_167244.1:g.3673882T>C, NT_167248.2:g.3614775T>C, NT_167248.1:g.3620371T>C, NT_167246.2:g.3696728T>C, NT_167246.1:g.3702348T>C, NT_167249.2:g.3707657T>C, NT_167249.1:g.3706955T>C, NT_167247.2:g.3733485T>C, NT_167247.1:g.3739070T>C, NT_167245.2:g.3632826T>C, NT_167245.1:g.3638411T>C, NT_187692.1:g.62225A>G, NR_044996.1:n.367T>C

Select item 14852979924.

rs1485297992 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32390678 (GRCh38)
6:32358455 (GRCh37)
Canonical SPDI:: NC_000006.12:32390677:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32390678A>G, NC_000006.11:g.32358455A>G, NT_113891.3:g.3828778A>G, NT_113891.2:g.3828884A>G, NT_167248.2:g.3613718A>G, NT_167248.1:g.3619314A>G, NT_167245.2:g.3631769A>G, NT_167245.1:g.3637354A>G, NT_167249.2:g.3706600A>G, NT_167249.1:g.3705898A>G, NT_167246.2:g.3695671A>G, NT_167246.1:g.3701291A>G, NT_167247.2:g.3732428A>G, NT_167247.1:g.3738013A>G, NT_167244.2:g.3722909A>G, NT_167244.1:g.3672825A>G, NT_187692.1:g.63288T>C, NR_044996.1:n.169A>G

Select item 14751503385.

rs1475150338 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:32393691 (GRCh38)
6:32361468 (GRCh37)
Canonical SPDI:: NC_000006.12:32393690:C:T
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32393691C>T, NC_000006.11:g.32361468C>T, NG_054759.1:g.20189G>A, NT_113891.3:g.3831783C>T, NT_113891.2:g.3831889C>T, NT_167244.2:g.3725922C>T, NT_167244.1:g.3675838C>T, NT_167248.2:g.3616730C>T, NT_167248.1:g.3622326C>T, NT_167246.2:g.3698684C>T, NT_167246.1:g.3704304C>T, NT_167249.2:g.3709613C>T, NT_167249.1:g.3708911C>T, NT_167247.2:g.3735441C>T, NT_167247.1:g.3741026C>T, NT_167245.2:g.3634782C>T, NT_167245.1:g.3640367C>T, NT_187692.1:g.60293G>A, NR_044996.1:n.615C>T

Select item 14526039206.

rs1452603920 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32393593 (GRCh38)
6:32361370 (GRCh37)
Canonical SPDI:: NC_000006.12:32393592:A:G
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000006.12:g.32393593A>G, NC_000006.11:g.32361370A>G, NG_054759.1:g.20287T>C, NT_113891.3:g.3831685A>G, NT_113891.2:g.3831791A>G, NT_167244.2:g.3725824A>G, NT_167244.1:g.3675740A>G, NT_167248.2:g.3616632A>G, NT_167248.1:g.3622228A>G, NT_167246.2:g.3698586A>G, NT_167246.1:g.3704206A>G, NT_167249.2:g.3709515A>G, NT_167249.1:g.3708813A>G, NT_167247.2:g.3735343A>G, NT_167247.1:g.3740928A>G, NT_167245.2:g.3634684A>G, NT_167245.1:g.3640269A>G, NT_187692.1:g.60388T>C, NR_044996.1:n.517A>G

Select item 14483121947.

rs1448312194 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 6:32390518 (GRCh38)
6:32358295 (GRCh37)
Canonical SPDI:: NC_000006.12:32390517:C:A,NC_000006.12:32390517:C:G,NC_000006.12:32390517:C:T
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.00004/1 (TOMMO)
HGVS:: NC_000006.12:g.32390518C>A, NC_000006.12:g.32390518C>G, NC_000006.12:g.32390518C>T, NC_000006.11:g.32358295C>A, NC_000006.11:g.32358295C>G, NC_000006.11:g.32358295C>T, NT_113891.3:g.3828618C>A, NT_113891.3:g.3828618C>G, NT_113891.3:g.3828618C>T, NT_113891.2:g.3828724C>A, NT_113891.2:g.3828724C>G, NT_113891.2:g.3828724C>T, NT_167248.2:g.3613558C>A, NT_167248.2:g.3613558C>G, NT_167248.2:g.3613558C>T, NT_167248.1:g.3619154C>A, NT_167248.1:g.3619154C>G, NT_167248.1:g.3619154C>T, NT_167245.2:g.3631609C>A, NT_167245.2:g.3631609C>G, NT_167245.2:g.3631609C>T, NT_167245.1:g.3637194C>A, NT_167245.1:g.3637194C>G, NT_167245.1:g.3637194C>T, NT_167249.2:g.3706439C>A, NT_167249.2:g.3706439C>G, NT_167249.2:g.3706439C>T, NT_167249.1:g.3705737C>A, NT_167249.1:g.3705737C>G, NT_167249.1:g.3705737C>T, NT_167246.2:g.3695510C>A, NT_167246.2:g.3695510C>G, NT_167246.2:g.3695510C>T, NT_167246.1:g.3701130C>A, NT_167246.1:g.3701130C>G, NT_167246.1:g.3701130C>T, NT_167247.2:g.3732267C>A, NT_167247.2:g.3732267C>G, NT_167247.2:g.3732267C>T, NT_167247.1:g.3737852C>A, NT_167247.1:g.3737852C>G, NT_167247.1:g.3737852C>T, NT_167244.2:g.3722749C>A, NT_167244.2:g.3722749C>G, NT_167244.2:g.3722749C>T, NT_167244.1:g.3672665C>A, NT_167244.1:g.3672665C>G, NT_167244.1:g.3672665C>T, NT_187692.1:g.63449G>T, NT_187692.1:g.63449G>C, NT_187692.1:g.63449G>A, NR_044996.1:n.9C>A, NR_044996.1:n.9C>G, NR_044996.1:n.9C>T

Select item 14463462168.

rs1446346216 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:32393557 (GRCh38)
6:32361334 (GRCh37)
Canonical SPDI:: NC_000006.12:32393556:G:C
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32393557G>C, NC_000006.11:g.32361334G>C, NG_054759.1:g.20323C>G, NT_113891.3:g.3831649G>C, NT_113891.2:g.3831755G>C, NT_167244.2:g.3725788G>C, NT_167244.1:g.3675704G>C, NT_167248.2:g.3616596G>C, NT_167248.1:g.3622192G>C, NT_167246.2:g.3698550G>C, NT_167246.1:g.3704170G>C, NT_167249.2:g.3709479G>C, NT_167249.1:g.3708777G>C, NT_167247.2:g.3735307G>C, NT_167247.1:g.3740892G>C, NT_167245.2:g.3634648G>C, NT_167245.1:g.3640233G>C, NT_187692.1:g.60424C>G, NR_044996.1:n.481G>C

Select item 14386602399.

rs1438660239 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:32391740 (GRCh38)
6:32359517 (GRCh37)
Canonical SPDI:: NC_000006.12:32391739:G:T
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000684/2 (KOREAN)
T=0.00184/31 (TOMMO)
HGVS:: NC_000006.12:g.32391740G>T, NC_000006.11:g.32359517G>T, NG_054759.1:g.22140C>A, NT_113891.3:g.3829840G>T, NT_113891.2:g.3829946G>T, NT_167244.2:g.3723971G>T, NT_167244.1:g.3673887G>T, NT_167248.2:g.3614780G>T, NT_167248.1:g.3620376G>T, NT_167246.2:g.3696733G>T, NT_167246.1:g.3702353G>T, NT_167249.2:g.3707662G>T, NT_167249.1:g.3706960G>T, NT_167247.2:g.3733490G>T, NT_167247.1:g.3739075G>T, NT_167245.2:g.3632831G>T, NT_167245.1:g.3638416G>T, NT_187692.1:g.62220C>A, not_yet_implemented, not_yet_implemented

Select item 143457143310.

rs1434571433 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32390611 (GRCh38)
6:32358388 (GRCh37)
Canonical SPDI:: NC_000006.12:32390610:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.32390611A>G, NC_000006.11:g.32358388A>G, NT_113891.3:g.3828711A>G, NT_113891.2:g.3828817A>G, NT_167248.2:g.3613651A>G, NT_167248.1:g.3619247A>G, NT_167245.2:g.3631702A>G, NT_167245.1:g.3637287A>G, NT_167249.2:g.3706532A>G, NT_167249.1:g.3705830A>G, NT_167246.2:g.3695603A>G, NT_167246.1:g.3701223A>G, NT_167247.2:g.3732360A>G, NT_167247.1:g.3737945A>G, NT_167244.2:g.3722842A>G, NT_167244.1:g.3672758A>G, NT_187692.1:g.63356T>C, NR_044996.1:n.102A>G

Select item 142068401811.

rs1420684018 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32390614 (GRCh38)
6:32358391 (GRCh37)
Canonical SPDI:: NC_000006.12:32390613:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32390614A>G, NC_000006.11:g.32358391A>G, NT_113891.3:g.3828714A>G, NT_113891.2:g.3828820A>G, NT_167248.2:g.3613654A>G, NT_167248.1:g.3619250A>G, NT_167245.2:g.3631705A>G, NT_167245.1:g.3637290A>G, NT_167249.2:g.3706535A>G, NT_167249.1:g.3705833A>G, NT_167246.2:g.3695606A>G, NT_167246.1:g.3701226A>G, NT_167247.2:g.3732363A>G, NT_167247.1:g.3737948A>G, NT_167244.2:g.3722845A>G, NT_167244.1:g.3672761A>G, NT_187692.1:g.63353T>C, NR_044996.1:n.105A>G

Select item 141998198012.

rs1419981980 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:32393477 (GRCh38)
6:32361254 (GRCh37)
Canonical SPDI:: NC_000006.12:32393476:C:T
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.32393477C>T, NC_000006.11:g.32361254C>T, NG_054759.1:g.20403G>A, NT_113891.3:g.3831569C>T, NT_113891.2:g.3831675C>T, NT_167244.2:g.3725708C>T, NT_167244.1:g.3675624C>T, NT_167248.2:g.3616516C>T, NT_167248.1:g.3622112C>T, NT_167246.2:g.3698470C>T, NT_167246.1:g.3704090C>T, NT_167249.2:g.3709399C>T, NT_167249.1:g.3708697C>T, NT_167247.2:g.3735227C>T, NT_167247.1:g.3740812C>T, NT_167245.2:g.3634568C>T, NT_167245.1:g.3640153C>T, NT_187692.1:g.60504G>A, NR_044996.1:n.401C>T

Select item 141747343813.

rs1417473438 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:32393473 (GRCh38)
6:32361250 (GRCh37)
Canonical SPDI:: NC_000006.12:32393472:C:T
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000053/1 (ALFA)
T=0./0 (KOREAN)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.32393473C>T, NC_000006.11:g.32361250C>T, NG_054759.1:g.20407G>A, NT_113891.3:g.3831565C>T, NT_113891.2:g.3831671C>T, NT_167244.2:g.3725704C>T, NT_167244.1:g.3675620C>T, NT_167248.2:g.3616512C>T, NT_167248.1:g.3622108C>T, NT_167246.2:g.3698466C>T, NT_167246.1:g.3704086C>T, NT_167249.2:g.3709395C>T, NT_167249.1:g.3708693C>T, NT_167247.2:g.3735223C>T, NT_167247.1:g.3740808C>T, NT_167245.2:g.3634564C>T, NT_167245.1:g.3640149C>T, NT_187692.1:g.60508G>A, NR_044996.1:n.397C>T

Select item 140633706814.

rs1406337068 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:32390718 (GRCh38)
6:32358495 (GRCh37)
Canonical SPDI:: NC_000006.12:32390717:C:A
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000026/7 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000006.12:g.32390718C>A, NC_000006.11:g.32358495C>A, NT_113891.3:g.3828818C>A, NT_113891.2:g.3828924C>A, NT_167248.2:g.3613758C>A, NT_167248.1:g.3619354C>A, NT_167245.2:g.3631809C>A, NT_167245.1:g.3637394C>A, NT_167249.2:g.3706640C>A, NT_167249.1:g.3705938C>A, NT_167246.2:g.3695711C>A, NT_167246.1:g.3701331C>A, NT_167247.2:g.3732468C>A, NT_167247.1:g.3738053C>A, NT_167244.2:g.3722949C>A, NT_167244.1:g.3672865C>A, NT_187692.1:g.63248G>T, NR_044996.1:n.209C>A

Select item 140368004115.

rs1403680041 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCA>- [Show Flanks]
Chromosome:: 6:32393564 (GRCh38)
6:32361341 (GRCh37)
Canonical SPDI:: NC_000006.12:32393561:CACCA:CA
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32393564_32393566del, NC_000006.11:g.32361341_32361343del, NG_054759.1:g.20316_20318del, NT_113891.3:g.3831656_3831658del, NT_113891.2:g.3831762_3831764del, NT_167244.2:g.3725795_3725797del, NT_167244.1:g.3675711_3675713del, NT_167248.2:g.3616603_3616605del, NT_167248.1:g.3622199_3622201del, NT_167246.2:g.3698557_3698559del, NT_167246.1:g.3704177_3704179del, NT_167249.2:g.3709486_3709488del, NT_167249.1:g.3708784_3708786del, NT_167247.2:g.3735314_3735316del, NT_167247.1:g.3740899_3740901del, NT_167245.2:g.3634655_3634657del, NT_167245.1:g.3640240_3640242del, NT_187692.1:g.60417_60419del, NR_044996.1:n.488_490del

Select item 140227656516.

rs1402276565 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 6:32393589 (GRCh38)
6:32361366 (GRCh37)
Canonical SPDI:: NC_000006.12:32393588:AAA:AA
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.32393591del, NC_000006.11:g.32361368del, NG_054759.1:g.20291del, NT_113891.3:g.3831683del, NT_113891.2:g.3831789del, NT_167244.2:g.3725822del, NT_167244.1:g.3675738del, NT_167248.2:g.3616630del, NT_167248.1:g.3622226del, NT_167246.2:g.3698584del, NT_167246.1:g.3704204del, NT_167249.2:g.3709513del, NT_167249.1:g.3708811del, NT_167247.2:g.3735341del, NT_167247.1:g.3740926del, NT_167245.2:g.3634682del, NT_167245.1:g.3640267del, NT_187692.1:g.60392del, NR_044996.1:n.515del

Select item 139835922817.

rs1398359228 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:32391703 (GRCh38)
6:32359480 (GRCh37)
Canonical SPDI:: NC_000006.12:32391702:G:A
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
A=0.000342/1 (KOREAN)
HGVS:: NC_000006.12:g.32391703G>A, NC_000006.11:g.32359480G>A, NG_054759.1:g.22177C>T, NT_113891.3:g.3829803G>A, NT_113891.2:g.3829909G>A, NT_167244.2:g.3723934G>A, NT_167244.1:g.3673850G>A, NT_167248.2:g.3614743G>A, NT_167248.1:g.3620339G>A, NT_167246.2:g.3696696G>A, NT_167246.1:g.3702316G>A, NT_167249.2:g.3707625G>A, NT_167249.1:g.3706923G>A, NT_167247.2:g.3733453G>A, NT_167247.1:g.3739038G>A, NT_167245.2:g.3632794G>A, NT_167245.1:g.3638379G>A, NT_187692.1:g.62257C>T, NR_044996.1:n.335G>A

Select item 138318396518.

rs1383183965 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32393589 (GRCh38)
6:32361366 (GRCh37)
Canonical SPDI:: NC_000006.12:32393588:A:G
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
HGVS:: NC_000006.12:g.32393589A>G, NC_000006.11:g.32361366A>G, NG_054759.1:g.20291T>C, NT_113891.3:g.3831681A>G, NT_113891.2:g.3831787A>G, NT_167244.2:g.3725820A>G, NT_167244.1:g.3675736A>G, NT_167248.2:g.3616628A>G, NT_167248.1:g.3622224A>G, NT_167246.2:g.3698582A>G, NT_167246.1:g.3704202A>G, NT_167249.2:g.3709511A>G, NT_167249.1:g.3708809A>G, NT_167247.2:g.3735339A>G, NT_167247.1:g.3740924A>G, NT_167245.2:g.3634680A>G, NT_167245.1:g.3640265A>G, NT_187692.1:g.60392T>C, NR_044996.1:n.513A>G

Select item 138279949219.

rs1382799492 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 6:32390510 (GRCh38)
6:32358287 (GRCh37)
Canonical SPDI:: NC_000006.12:32390509:G:A,NC_000006.12:32390509:G:C
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.00003/8 (TOPMED)
A=0.000248/4 (TOMMO)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000006.12:g.32390510G>A, NC_000006.12:g.32390510G>C, NC_000006.11:g.32358287G>A, NC_000006.11:g.32358287G>C, NT_113891.3:g.3828610G>A, NT_113891.3:g.3828610G>C, NT_113891.2:g.3828716G>A, NT_113891.2:g.3828716G>C, NT_167248.2:g.3613550G>A, NT_167248.2:g.3613550G>C, NT_167248.1:g.3619146G>A, NT_167248.1:g.3619146G>C, NT_167245.2:g.3631601G>A, NT_167245.2:g.3631601G>C, NT_167245.1:g.3637186G>A, NT_167245.1:g.3637186G>C, NT_167249.2:g.3706431G>A, NT_167249.2:g.3706431G>C, NT_167249.1:g.3705729G>A, NT_167249.1:g.3705729G>C, NT_167246.2:g.3695502G>A, NT_167246.2:g.3695502G>C, NT_167246.1:g.3701122G>A, NT_167246.1:g.3701122G>C, NT_167247.2:g.3732259G>A, NT_167247.2:g.3732259G>C, NT_167247.1:g.3737844G>A, NT_167247.1:g.3737844G>C, NT_167244.2:g.3722741G>A, NT_167244.2:g.3722741G>C, NT_167244.1:g.3672657G>A, NT_167244.1:g.3672657G>C, NT_187692.1:g.63457C>T, NT_187692.1:g.63457C>G, NR_044996.1:n.1G>A, NR_044996.1:n.1G>C

Select item 138135300520.

rs1381353005 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:32393690 (GRCh38)
6:32361467 (GRCh37)
Canonical SPDI:: NC_000006.12:32393689:C:G
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.32393690C>G, NC_000006.11:g.32361467C>G, NG_054759.1:g.20190G>C, NT_113891.3:g.3831782C>G, NT_113891.2:g.3831888C>G, NT_167244.2:g.3725921C>G, NT_167244.1:g.3675837C>G, NT_167248.2:g.3616729C>G, NT_167248.1:g.3622325C>G, NT_167246.2:g.3698683C>G, NT_167246.1:g.3704303C>G, NT_167249.2:g.3709612C>G, NT_167249.1:g.3708910C>G, NT_167247.2:g.3735440C>G, NT_167247.1:g.3741025C>G, NT_167245.2:g.3634781C>G, NT_167245.1:g.3640366C>G, NR_044996.1:n.614C>G

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