SNP Links for Nucleotide (Select 533874078) - SNP

Links from Nucleotide

Items: 1 to 20 of 126

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Select item 14898589351.

rs1489858935 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 13:29918696 (GRCh38)
13:30492833 (GRCh37)
Canonical SPDI:: NC_000013.11:29918695:A:C,NC_000013.11:29918695:A:G
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.29918696A>C, NC_000013.11:g.29918696A>G, NC_000013.10:g.30492833A>C, NC_000013.10:g.30492833A>G, NR_047501.1:n.526T>G, NR_047501.1:n.526T>C

Select item 14815881912.

rs1481588191 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:29918913 (GRCh38)
13:30493050 (GRCh37)
Canonical SPDI:: NC_000013.11:29918912:G:A
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.00003/8 (TOPMED)
HGVS:: NC_000013.11:g.29918913G>A, NC_000013.10:g.30493050G>A, NR_047501.1:n.309C>T

Select item 14796135943.

rs1479613594 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:29918671 (GRCh38)
13:30492808 (GRCh37)
Canonical SPDI:: NC_000013.11:29918670:T:C
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000064/9 (GnomAD)
HGVS:: NC_000013.11:g.29918671T>C, NC_000013.10:g.30492808T>C, NR_047501.1:n.551A>G

Select item 14794037394.

rs1479403739 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:29918769 (GRCh38)
13:30492906 (GRCh37)
Canonical SPDI:: NC_000013.11:29918768:G:T
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.29918769G>T, NC_000013.10:g.30492906G>T, NR_047501.1:n.453C>A

Select item 14790002565.

rs1479000256 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 13:29918936 (GRCh38)
13:30493073 (GRCh37)
Canonical SPDI:: NC_000013.11:29918935:T:C,NC_000013.11:29918935:T:G
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.29918936T>C, NC_000013.11:g.29918936T>G, NC_000013.10:g.30493073T>C, NC_000013.10:g.30493073T>G, NR_047501.1:n.286A>G, NR_047501.1:n.286A>C

Select item 14644268866.

rs1464426886 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 13:29926509 (GRCh38)
13:30500646 (GRCh37)
Canonical SPDI:: NC_000013.11:29926508:G:A,NC_000013.11:29926508:G:T
Gene:: LINC00572 (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)
A=0.000035/1 (TOMMO)
HGVS:: NC_000013.11:g.29926509G>A, NC_000013.11:g.29926509G>T, NC_000013.10:g.30500646G>A, NC_000013.10:g.30500646G>T, NR_047501.1:n.143C>T, NR_047501.1:n.143C>A

Select item 14619113037.

rs1461911303 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:29918724 (GRCh38)
13:30492861 (GRCh37)
Canonical SPDI:: NC_000013.11:29918723:A:G
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000013.11:g.29918724A>G, NC_000013.10:g.30492861A>G, NR_047501.1:n.498T>C

Select item 14567745728.

rs1456774572 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:29918923 (GRCh38)
13:30493060 (GRCh37)
Canonical SPDI:: NC_000013.11:29918922:C:T
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.0005/1 (Korea1K)
HGVS:: NC_000013.11:g.29918923C>T, NC_000013.10:g.30493060C>T, NR_047501.1:n.299G>A

Select item 14548699699.

rs1454869969 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:29918955 (GRCh38)
13:30493092 (GRCh37)
Canonical SPDI:: NC_000013.11:29918954:G:T
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000013.11:g.29918955G>T, NC_000013.10:g.30493092G>T, NR_047501.1:n.267C>A

Select item 144482908110.

rs1444829081 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:29918684 (GRCh38)
13:30492821 (GRCh37)
Canonical SPDI:: NC_000013.11:29918683:C:T
Gene:: LINC00572 (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=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.29918684C>T, NC_000013.10:g.30492821C>T, NR_047501.1:n.538G>A

Select item 144196343011.

rs1441963430 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:29919017 (GRCh38)
13:30493154 (GRCh37)
Canonical SPDI:: NC_000013.11:29919016:C:A
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.29919017C>A, NC_000013.10:g.30493154C>A, NR_047501.1:n.205G>T

Select item 144115328212.

rs1441153282 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 13:29919070 (GRCh38)
13:30493207 (GRCh37)
Canonical SPDI:: NC_000013.11:29919069:T:C,NC_000013.11:29919069:T:G
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.000007/1 (GnomAD)
G=0.001092/2 (Korea1K)
HGVS:: NC_000013.11:g.29919070T>C, NC_000013.11:g.29919070T>G, NC_000013.10:g.30493207T>C, NC_000013.10:g.30493207T>G, NR_047501.1:n.152A>G, NR_047501.1:n.152A>C

Select item 143743607613.

rs1437436076 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 13:29918947 (GRCh38)
13:30493084 (GRCh37)
Canonical SPDI:: NC_000013.11:29918946:A:T
Gene:: LINC00572 (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_000013.11:g.29918947A>T, NC_000013.10:g.30493084A>T, NR_047501.1:n.275T>A

Select item 143368129214.

rs1433681292 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:29926527 (GRCh38)
13:30500664 (GRCh37)
Canonical SPDI:: NC_000013.11:29926526:G:A
Gene:: LINC00572 (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_000013.11:g.29926527G>A, NC_000013.10:g.30500664G>A, NR_047501.1:n.125C>T

Select item 142184223515.

rs1421842235 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:29918666 (GRCh38)
13:30492803 (GRCh37)
Canonical SPDI:: NC_000013.11:29918665:T:G
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.29918666T>G, NC_000013.10:g.30492803T>G, NR_047501.1:n.556A>C

Select item 141606741016.

rs1416067410 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:29919060 (GRCh38)
13:30493197 (GRCh37)
Canonical SPDI:: NC_000013.11:29919059:T:C
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.29919060T>C, NC_000013.10:g.30493197T>C, NR_047501.1:n.162A>G

Select item 140635445917.

rs1406354459 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:29918747 (GRCh38)
13:30492884 (GRCh37)
Canonical SPDI:: NC_000013.11:29918746:C:T
Gene:: LINC00572 (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_000013.11:g.29918747C>T, NC_000013.10:g.30492884C>T, NR_047501.1:n.475G>A

Select item 140575984218.

rs1405759842 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:29919066 (GRCh38)
13:30493203 (GRCh37)
Canonical SPDI:: NC_000013.11:29919065:C:T
Gene:: LINC00572 (Varview)
Functional Consequence:: 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)
HGVS:: NC_000013.11:g.29919066C>T, NC_000013.10:g.30493203C>T, NR_047501.1:n.156G>A

Select item 140238977119.

rs1402389771 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 13:29918736 (GRCh38)
13:30492873 (GRCh37)
Canonical SPDI:: NC_000013.11:29918735:G:A,NC_000013.11:29918735:G:T
Gene:: LINC00572 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.29918736G>A, NC_000013.11:g.29918736G>T, NC_000013.10:g.30492873G>A, NC_000013.10:g.30492873G>T, NR_047501.1:n.486C>T, NR_047501.1:n.486C>A

Select item 140064111920.

rs1400641119 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:29918910 (GRCh38)
13:30493047 (GRCh37)
Canonical SPDI:: NC_000013.11:29918909:G:T
Gene:: LINC00572 (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=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.29918910G>T, NC_000013.10:g.30493047G>T, NR_047501.1:n.312C>A

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