SNP Links for Nucleotide (Select 1077231791) - SNP

Links from Nucleotide

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Select item 14866065501.

rs1486606550 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:33117068 (GRCh38)
6:33084846 (GRCh37)
Canonical SPDI:: NC_000006.12:33117068:GGGGG:GGGGGG
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGG=0./0 (ALFA)
G=0.00031/2 (1000Genomes)
HGVS:: NC_000006.12:g.33117073dup, NC_000006.11:g.33084850dup, NT_113891.3:g.4528853dup, NT_113891.2:g.4528959dup, NT_167248.2:g.4311746dup, NT_167248.1:g.4317342dup, NT_167249.2:g.4566039dup, NT_167249.1:g.4565337dup, NT_167246.2:g.4536815dup, NT_167246.1:g.4542435dup, NT_167247.2:g.4416082dup, NT_167247.1:g.4421667dup, NT_167244.2:g.4421697dup, NT_167244.1:g.4371613dup, NR_001435.2:n.217dup, NR_001435.1:n.217dup

Select item 14860661252.

rs1486066125 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:33116965 (GRCh38)
6:33084742 (GRCh37)
Canonical SPDI:: NC_000006.12:33116964:G:C
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000006.12:g.33116965G>C, NC_000006.11:g.33084742G>C, NT_113891.3:g.4528745G>C, NT_113891.2:g.4528851G>C, NT_167248.2:g.4311638G>C, NT_167248.1:g.4317234G>C, NT_167249.2:g.4565931G>C, NT_167249.1:g.4565229G>C, NT_167246.2:g.4536707G>C, NT_167246.1:g.4542327G>C, NT_167247.2:g.4415974G>C, NT_167247.1:g.4421559G>C, NT_167244.2:g.4421589G>C, NT_167244.1:g.4371505G>C, NR_001435.2:n.109G>C, NR_001435.1:n.109G>C

Select item 14855460883.

rs1485546088 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 6:33117037 (GRCh38)
6:33084814 (GRCh37)
Canonical SPDI:: NC_000006.12:33117036:C:G,NC_000006.12:33117036:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.00004/1 (TOMMO)
HGVS:: NC_000006.12:g.33117037C>G, NC_000006.12:g.33117037C>T, NC_000006.11:g.33084814C>G, NC_000006.11:g.33084814C>T, NT_113891.3:g.4528817C>G, NT_113891.3:g.4528817C>T, NT_113891.2:g.4528923C>G, NT_113891.2:g.4528923C>T, NT_167248.2:g.4311710C>G, NT_167248.2:g.4311710C>T, NT_167248.1:g.4317306C>G, NT_167248.1:g.4317306C>T, NT_167249.2:g.4566003C>G, NT_167249.2:g.4566003C>T, NT_167249.1:g.4565301C>G, NT_167249.1:g.4565301C>T, NT_167246.2:g.4536779C>G, NT_167246.2:g.4536779C>T, NT_167246.1:g.4542399C>G, NT_167246.1:g.4542399C>T, NT_167247.2:g.4416046C>G, NT_167247.2:g.4416046C>T, NT_167247.1:g.4421631C>G, NT_167247.1:g.4421631C>T, NT_167244.2:g.4421661C>G, NT_167244.2:g.4421661C>T, NT_167244.1:g.4371577C>G, NT_167244.1:g.4371577C>T, NR_001435.2:n.181C>G, NR_001435.2:n.181C>T, NR_001435.1:n.181C>G, NR_001435.1:n.181C>T

Select item 14812098884.

rs1481209888 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:33128700 (GRCh38)
6:33096477 (GRCh37)
Canonical SPDI:: NC_000006.12:33128699:T:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.33128700T>A, NC_000006.11:g.33096477T>A, NT_113891.3:g.4540159T>A, NT_113891.2:g.4540265T>A, NT_167248.2:g.4323051T>A, NT_167248.1:g.4328647T>A, NT_167245.2:g.4372198T>A, NT_167245.1:g.4377783T>A, NT_167249.2:g.4577344T>A, NT_167249.1:g.4576642T>A, NT_167246.2:g.4548120T>A, NT_167246.1:g.4553740T>A, NT_167244.2:g.4433321T>A, NT_167244.1:g.4383237T>A, NR_001435.2:n.712T>A, NR_001435.1:n.712T>A, XR_007068748.1:n.6025A>T

Select item 14780089745.

rs1478008974 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:33128689 (GRCh38)
6:33096466 (GRCh37)
Canonical SPDI:: NC_000006.12:33128688:G:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_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_000006.12:g.33128689G>A, NC_000006.11:g.33096466G>A, NT_113891.3:g.4540148G>A, NT_113891.2:g.4540254G>A, NT_167248.2:g.4323040G>A, NT_167248.1:g.4328636G>A, NT_167245.2:g.4372187G>A, NT_167245.1:g.4377772G>A, NT_167249.2:g.4577333G>A, NT_167249.1:g.4576631G>A, NT_167246.2:g.4548109G>A, NT_167246.1:g.4553729G>A, NT_167244.2:g.4433310G>A, NT_167244.1:g.4383226G>A, NR_001435.2:n.701G>A, NR_001435.1:n.701G>A, XR_007068748.1:n.6036C>T

Select item 14766341786.

rs1476634178 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33127839 (GRCh38)
6:33095616 (GRCh37)
Canonical SPDI:: NC_000006.12:33127838:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.33127839C>T, NC_000006.11:g.33095616C>T, NT_113891.3:g.4539298C>T, NT_113891.2:g.4539404C>T, NT_167248.2:g.4322190C>T, NT_167248.1:g.4327786C>T, NT_167245.2:g.4371337C>T, NT_167245.1:g.4376922C>T, NT_167249.2:g.4576483C>T, NT_167249.1:g.4575781C>T, NT_167246.2:g.4547259C>T, NT_167246.1:g.4552879C>T, NT_167244.2:g.4432460C>T, NT_167244.1:g.4382376C>T, NR_001435.2:n.386C>T, NR_001435.1:n.386C>T

Select item 14765626547.

rs1476562654 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33127885 (GRCh38)
6:33095662 (GRCh37)
Canonical SPDI:: NC_000006.12:33127884:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_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_000006.12:g.33127885C>T, NC_000006.11:g.33095662C>T, NT_113891.3:g.4539344C>T, NT_113891.2:g.4539450C>T, NT_167248.2:g.4322236C>T, NT_167248.1:g.4327832C>T, NT_167245.2:g.4371383C>T, NT_167245.1:g.4376968C>T, NT_167249.2:g.4576529C>T, NT_167249.1:g.4575827C>T, NT_167246.2:g.4547305C>T, NT_167246.1:g.4552925C>T, NT_167244.2:g.4432506C>T, NT_167244.1:g.4382422C>T, NR_001435.2:n.432C>T, NR_001435.1:n.432C>T, XR_007068748.1:n.6840G>A

Select item 14723063368.

rs1472306336 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33128043 (GRCh38)
6:33095820 (GRCh37)
Canonical SPDI:: NC_000006.12:33128042:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000029/4 (GnomAD)
T=0.000042/11 (TOPMED)
HGVS:: NC_000006.12:g.33128043C>T, NC_000006.11:g.33095820C>T, NT_113891.3:g.4539502C>T, NT_113891.2:g.4539608C>T, NT_167248.2:g.4322394C>T, NT_167248.1:g.4327990C>T, NT_167245.2:g.4371541C>T, NT_167245.1:g.4377126C>T, NT_167249.2:g.4576687C>T, NT_167249.1:g.4575985C>T, NT_167246.2:g.4547463C>T, NT_167246.1:g.4553083C>T, NT_167244.2:g.4432664C>T, NT_167244.1:g.4382580C>T, NR_001435.2:n.590C>T, NR_001435.1:n.590C>T, XR_007068748.1:n.6682G>A

Select item 14700563189.

rs1470056318 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:33117129 (GRCh38)
6:33084906 (GRCh37)
Canonical SPDI:: NC_000006.12:33117128:G:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000006.12:g.33117129G>A, NC_000006.11:g.33084906G>A, NT_113891.3:g.4528909G>A, NT_113891.2:g.4529015G>A, NT_167248.2:g.4311802G>A, NT_167248.1:g.4317398G>A, NT_167249.2:g.4566095G>A, NT_167249.1:g.4565393G>A, NT_167246.2:g.4536871G>A, NT_167246.1:g.4542491G>A, NT_167247.2:g.4416138G>A, NT_167247.1:g.4421723G>A, NT_167244.2:g.4421753G>A, NT_167244.1:g.4371669G>A, NR_001435.2:n.273G>A, NR_001435.1:n.273G>A

Select item 146774641910.

rs1467746419 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:33112589 (GRCh38)
6:33080366 (GRCh37)
Canonical SPDI:: NC_000006.12:33112588:C:A,NC_000006.12:33112588:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.33112589C>A, NC_000006.12:g.33112589C>T, NC_000006.11:g.33080366C>A, NC_000006.11:g.33080366C>T, NT_113891.3:g.4524360C>A, NT_113891.3:g.4524360C>T, NT_113891.2:g.4524466C>A, NT_113891.2:g.4524466C>T, NT_167248.2:g.4307225C>A, NT_167248.2:g.4307225C>T, NT_167248.1:g.4312821C>A, NT_167248.1:g.4312821C>T, NT_167249.2:g.4561546C>A, NT_167249.2:g.4561546C>T, NT_167249.1:g.4560844C>A, NT_167249.1:g.4560844C>T, NT_167246.2:g.4532294C>A, NT_167246.2:g.4532294C>T, NT_167246.1:g.4537914C>A, NT_167246.1:g.4537914C>T, NT_167247.2:g.4411599C>A, NT_167247.2:g.4411599C>T, NT_167247.1:g.4417184C>A, NT_167247.1:g.4417184C>T, NT_167244.2:g.4417214C>A, NT_167244.2:g.4417214C>T, NT_167244.1:g.4367130C>A, NT_167244.1:g.4367130C>T, NR_001435.2:n.74C>A, NR_001435.2:n.74C>T, NR_001435.1:n.74C>A, NR_001435.1:n.74C>T

Select item 146745574211.

rs1467455742 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:33117062 (GRCh38)
6:33084839 (GRCh37)
Canonical SPDI:: NC_000006.12:33117061:G:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.33117062G>A, NC_000006.11:g.33084839G>A, NT_113891.3:g.4528842G>A, NT_113891.2:g.4528948G>A, NT_167248.2:g.4311735G>A, NT_167248.1:g.4317331G>A, NT_167249.2:g.4566028G>A, NT_167249.1:g.4565326G>A, NT_167246.2:g.4536804G>A, NT_167246.1:g.4542424G>A, NT_167247.2:g.4416071G>A, NT_167247.1:g.4421656G>A, NT_167244.2:g.4421686G>A, NT_167244.1:g.4371602G>A, NR_001435.2:n.206G>A, NR_001435.1:n.206G>A

Select item 145362513812.

rs1453625138 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:33112536 (GRCh38)
6:33080314 (GRCh37)
Canonical SPDI:: NC_000006.12:33112536:GGGGG:GGGGGG
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000006.12:g.33112541dup, NC_000006.11:g.33080318dup, NT_113891.3:g.4524312dup, NT_113891.2:g.4524418dup, NT_167248.2:g.4307177dup, NT_167248.1:g.4312773dup, NT_167249.2:g.4561498dup, NT_167249.1:g.4560796dup, NT_167246.2:g.4532246dup, NT_167246.1:g.4537866dup, NT_167247.2:g.4411551dup, NT_167247.1:g.4417136dup, NT_167244.2:g.4417166dup, NT_167244.1:g.4367082dup, NR_001435.2:n.26dup, NR_001435.1:n.23C>G, NR_001435.1:n.23delinsGG

Select item 145238571813.

rs1452385718 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:33117088 (GRCh38)
6:33084865 (GRCh37)
Canonical SPDI:: NC_000006.12:33117087:A:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.33117088A>T, NC_000006.11:g.33084865A>T, NT_113891.3:g.4528868A>T, NT_113891.2:g.4528974A>T, NT_167248.2:g.4311761A>T, NT_167248.1:g.4317357A>T, NT_167249.2:g.4566054A>T, NT_167249.1:g.4565352A>T, NT_167246.2:g.4536830A>T, NT_167246.1:g.4542450A>T, NT_167247.2:g.4416097A>T, NT_167247.1:g.4421682A>T, NT_167244.2:g.4421712A>T, NT_167244.1:g.4371628A>T, NR_001435.2:n.232A>T, NR_001435.1:n.232A>T

Select item 145110452414.

rs1451104524 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33127869 (GRCh38)
6:33095646 (GRCh37)
Canonical SPDI:: NC_000006.12:33127868:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000049/13 (TOPMED)
T=0.000071/10 (GnomAD)
HGVS:: NC_000006.12:g.33127869C>T, NC_000006.11:g.33095646C>T, NT_113891.3:g.4539328C>T, NT_113891.2:g.4539434C>T, NT_167248.2:g.4322220C>T, NT_167248.1:g.4327816C>T, NT_167245.2:g.4371367C>T, NT_167245.1:g.4376952C>T, NT_167249.2:g.4576513C>T, NT_167249.1:g.4575811C>T, NT_167246.2:g.4547289C>T, NT_167246.1:g.4552909C>T, NT_167244.2:g.4432490C>T, NT_167244.1:g.4382406C>T, NR_001435.2:n.416C>T, NR_001435.1:n.416C>T, XR_007068748.1:n.6856G>A

Select item 144984296315.

rs1449842963 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 6:33128010 (GRCh38)
6:33095787 (GRCh37)
Canonical SPDI:: NC_000006.12:33128009:G:A,NC_000006.12:33128009:G:C
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000155/41 (TOPMED)
HGVS:: NC_000006.12:g.33128010G>A, NC_000006.12:g.33128010G>C, NC_000006.11:g.33095787G>A, NC_000006.11:g.33095787G>C, NT_113891.3:g.4539469G>A, NT_113891.3:g.4539469G>C, NT_113891.2:g.4539575G>A, NT_113891.2:g.4539575G>C, NT_167248.2:g.4322361G>A, NT_167248.2:g.4322361G>C, NT_167248.1:g.4327957G>A, NT_167248.1:g.4327957G>C, NT_167245.2:g.4371508G>A, NT_167245.2:g.4371508G>C, NT_167245.1:g.4377093G>A, NT_167245.1:g.4377093G>C, NT_167249.2:g.4576654G>A, NT_167249.2:g.4576654G>C, NT_167249.1:g.4575952G>A, NT_167249.1:g.4575952G>C, NT_167246.2:g.4547430G>A, NT_167246.2:g.4547430G>C, NT_167246.1:g.4553050G>A, NT_167246.1:g.4553050G>C, NT_167244.2:g.4432631G>A, NT_167244.2:g.4432631G>C, NT_167244.1:g.4382547G>A, NT_167244.1:g.4382547G>C, NR_001435.2:n.557G>A, NR_001435.2:n.557G>C, NR_001435.1:n.557G>A, NR_001435.1:n.557G>C, XR_007068748.1:n.6715C>T, XR_007068748.1:n.6715C>G

Select item 144962866916.

rs1449628669 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:33128056 (GRCh38)
6:33095833 (GRCh37)
Canonical SPDI:: NC_000006.12:33128055:G:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.33128056G>A, NC_000006.11:g.33095833G>A, NT_113891.3:g.4539515G>A, NT_113891.2:g.4539621G>A, NT_167248.2:g.4322407G>A, NT_167248.1:g.4328003G>A, NT_167245.2:g.4371554G>A, NT_167245.1:g.4377139G>A, NT_167249.2:g.4576700G>A, NT_167249.1:g.4575998G>A, NT_167246.2:g.4547476G>A, NT_167246.1:g.4553096G>A, NT_167244.2:g.4432677G>A, NT_167244.1:g.4382593G>A, NR_001435.2:n.603G>A, NR_001435.1:n.603G>A, XR_007068748.1:n.6669C>T

Select item 144946201917.

rs1449462019 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:33117048 (GRCh38)
6:33084825 (GRCh37)
Canonical SPDI:: NC_000006.12:33117047:C:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.33117048C>A, NC_000006.11:g.33084825C>A, NT_113891.3:g.4528828C>A, NT_113891.2:g.4528934C>A, NT_167248.2:g.4311721C>A, NT_167248.1:g.4317317C>A, NT_167249.2:g.4566014C>A, NT_167249.1:g.4565312C>A, NT_167246.2:g.4536790C>A, NT_167246.1:g.4542410C>A, NT_167247.2:g.4416057C>A, NT_167247.1:g.4421642C>A, NT_167244.2:g.4421672C>A, NT_167244.1:g.4371588C>A, NR_001435.2:n.192C>A, NR_001435.1:n.192C>A

Select item 144700916118.

rs1447009161 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:33112521 (GRCh38)
6:33080298 (GRCh37)
Canonical SPDI:: NC_000006.12:33112520:G:A
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000013/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.33112521G>A, NC_000006.11:g.33080298G>A, NT_113891.3:g.4524292G>A, NT_113891.2:g.4524398G>A, NT_167248.2:g.4307157G>A, NT_167248.1:g.4312753G>A, NT_167249.2:g.4561478G>A, NT_167249.1:g.4560776G>A, NT_167246.2:g.4532226G>A, NT_167246.1:g.4537846G>A, NT_167247.2:g.4411531G>A, NT_167247.1:g.4417116G>A, NT_167244.2:g.4417146G>A, NT_167244.1:g.4367062G>A, NR_001435.2:n.6G>A, NR_001435.1:n.6G>A

Select item 144269650119.

rs1442696501 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:33127858 (GRCh38)
6:33095635 (GRCh37)
Canonical SPDI:: NC_000006.12:33127857:C:T
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000006.12:g.33127858C>T, NC_000006.11:g.33095635C>T, NT_113891.3:g.4539317C>T, NT_113891.2:g.4539423C>T, NT_167248.2:g.4322209C>T, NT_167248.1:g.4327805C>T, NT_167245.2:g.4371356C>T, NT_167245.1:g.4376941C>T, NT_167249.2:g.4576502C>T, NT_167249.1:g.4575800C>T, NT_167246.2:g.4547278C>T, NT_167246.1:g.4552898C>T, NT_167244.2:g.4432479C>T, NT_167244.1:g.4382395C>T, NR_001435.2:n.405C>T, NR_001435.1:n.405C>T

Select item 144215120820.

rs1442151208 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 6:33112572 (GRCh38)
6:33080349 (GRCh37)
Canonical SPDI:: NC_000006.12:33112571:G:A,NC_000006.12:33112571:G:C
Gene:: HLA-DPB2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
C=0.000006/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
C=0.000342/1 (KOREAN)
HGVS:: NC_000006.12:g.33112572G>A, NC_000006.12:g.33112572G>C, NC_000006.11:g.33080349G>A, NC_000006.11:g.33080349G>C, NT_113891.3:g.4524343G>A, NT_113891.3:g.4524343G>C, NT_113891.2:g.4524449G>A, NT_113891.2:g.4524449G>C, NT_167248.2:g.4307208G>A, NT_167248.2:g.4307208G>C, NT_167248.1:g.4312804G>A, NT_167248.1:g.4312804G>C, NT_167249.2:g.4561529G>A, NT_167249.2:g.4561529G>C, NT_167249.1:g.4560827G>A, NT_167249.1:g.4560827G>C, NT_167246.2:g.4532277G>A, NT_167246.2:g.4532277G>C, NT_167246.1:g.4537897G>A, NT_167246.1:g.4537897G>C, NT_167247.2:g.4411582G>A, NT_167247.2:g.4411582G>C, NT_167247.1:g.4417167G>A, NT_167247.1:g.4417167G>C, NT_167244.2:g.4417197G>A, NT_167244.2:g.4417197G>C, NT_167244.1:g.4367113G>A, NT_167244.1:g.4367113G>C, NR_001435.2:n.57G>A, NR_001435.2:n.57G>C, NR_001435.1:n.57G>A, NR_001435.1:n.57G>C

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