SNP Links for Nucleotide (Select 223555993) - SNP

Links from Nucleotide

Items: 1 to 20 of 826

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Select item 14878983231.

rs1487898323 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:5987970 (GRCh38)
2:6128102 (GRCh37)
Canonical SPDI:: NC_000002.12:5987969:A:G
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000058/8 (GnomAD)
G=0.00006/16 (TOPMED)
HGVS:: NC_000002.12:g.5987970A>G, NC_000002.11:g.6128102A>G, NR_026833.1:n.3201A>G

Select item 14868853992.

rs1486885399 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:5987759 (GRCh38)
2:6127891 (GRCh37)
Canonical SPDI:: NC_000002.12:5987758:C:A
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000034/9 (TOPMED)
HGVS:: NC_000002.12:g.5987759C>A, NC_000002.11:g.6127891C>A, NR_026833.1:n.2990C>A

Select item 14868580993.

rs1486858099 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:5987169 (GRCh38)
2:6127301 (GRCh37)
Canonical SPDI:: NC_000002.12:5987168:G:A
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.5987169G>A, NC_000002.11:g.6127301G>A, NR_026833.1:n.2400G>A

Select item 14854446964.

rs1485444696 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:5987752 (GRCh38)
2:6127884 (GRCh37)
Canonical SPDI:: NC_000002.12:5987751:G:A
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.5987752G>A, NC_000002.11:g.6127884G>A, NR_026833.1:n.2983G>A

Select item 14845664855.

rs1484566485 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:5987634 (GRCh38)
2:6127766 (GRCh37)
Canonical SPDI:: NC_000002.12:5987633:G:A
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.5987634G>A, NC_000002.11:g.6127766G>A, NR_026833.1:n.2865G>A

Select item 14840526406.

rs1484052640 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:5985655 (GRCh38)
2:6125787 (GRCh37)
Canonical SPDI:: NC_000002.12:5985654:A:C
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.5985655A>C, NC_000002.11:g.6125787A>C, NR_026833.1:n.886A>C

Select item 14826572397.

rs1482657239 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 2:5986057 (GRCh38)
2:6126189 (GRCh37)
Canonical SPDI:: NC_000002.12:5986056:CC:C
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: CC=0.000071/1 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.5986058del, NC_000002.11:g.6126190del, NR_026833.1:n.1289del

Select item 14824146428.

rs1482414642 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:5982645 (GRCh38)
2:6122777 (GRCh37)
Canonical SPDI:: NC_000002.12:5982644:G:A
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.5982645G>A, NC_000002.11:g.6122777G>A, NR_026833.1:n.443G>A, NM_207479.1:c.-289G>A

Select item 14806828959.

rs1480682895 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:5982715 (GRCh38)
2:6122847 (GRCh37)
Canonical SPDI:: NC_000002.12:5982714:C:T
Gene:: LOC400940 (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_000002.12:g.5982715C>T, NC_000002.11:g.6122847C>T, NR_026833.1:n.513C>T, NM_207479.1:c.-219C>T

Select item 147942706010.

rs1479427060 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:5987951 (GRCh38)
2:6128083 (GRCh37)
Canonical SPDI:: NC_000002.12:5987950:C:G
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000342/1 (KOREAN)
HGVS:: NC_000002.12:g.5987951C>G, NC_000002.11:g.6128083C>G, NR_026833.1:n.3182C>G

Select item 147934218411.

rs1479342184 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:5987830 (GRCh38)
2:6127962 (GRCh37)
Canonical SPDI:: NC_000002.12:5987829:C:T
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000002.12:g.5987830C>T, NC_000002.11:g.6127962C>T, NR_026833.1:n.3061C>T

Select item 147687123912.

rs1476871239 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 2:5985545 (GRCh38)
2:6125677 (GRCh37)
Canonical SPDI:: NC_000002.12:5985544:C:A,NC_000002.12:5985544:C:T
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000002.12:g.5985545C>A, NC_000002.12:g.5985545C>T, NC_000002.11:g.6125677C>A, NC_000002.11:g.6125677C>T, NR_026833.1:n.776C>A, NR_026833.1:n.776C>T

Select item 147359977813.

rs1473599778 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:5982851 (GRCh38)
2:6122983 (GRCh37)
Canonical SPDI:: NC_000002.12:5982850:A:G
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.5982851A>G, NC_000002.11:g.6122983A>G, NR_026833.1:n.649A>G, NM_207479.1:c.-83A>G

Select item 147311657314.

rs1473116573 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:5985440 (GRCh38)
2:6125572 (GRCh37)
Canonical SPDI:: NC_000002.12:5985439:A:G
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000002.12:g.5985440A>G, NC_000002.11:g.6125572A>G, NR_026833.1:n.671A>G

Select item 147230636615.

rs1472306366 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:5986628 (GRCh38)
2:6126760 (GRCh37)
Canonical SPDI:: NC_000002.12:5986627:G:C
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000036/5 (GnomAD)
HGVS:: NC_000002.12:g.5986628G>C, NC_000002.11:g.6126760G>C, NR_026833.1:n.1859G>C

Select item 147225271616.

rs1472252716 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:5985988 (GRCh38)
2:6126120 (GRCh37)
Canonical SPDI:: NC_000002.12:5985987:C:T
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00016/1 (1000Genomes)
T=0.00055/1 (Korea1K)
HGVS:: NC_000002.12:g.5985988C>T, NC_000002.11:g.6126120C>T, NR_026833.1:n.1219C>T

Select item 147183303917.

rs1471833039 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:5985751 (GRCh38)
2:6125883 (GRCh37)
Canonical SPDI:: NC_000002.12:5985750:G:A
Gene:: LOC400940 (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_000002.12:g.5985751G>A, NC_000002.11:g.6125883G>A, NR_026833.1:n.982G>A

Select item 147122421218.

rs1471224212 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:5987617 (GRCh38)
2:6127749 (GRCh37)
Canonical SPDI:: NC_000002.12:5987616:A:G
Gene:: LOC400940 (Varview)
Functional Consequence:: 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_000002.12:g.5987617A>G, NC_000002.11:g.6127749A>G, NR_026833.1:n.2848A>G

Select item 146946097119.

rs1469460971 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:5987889 (GRCh38)
2:6128021 (GRCh37)
Canonical SPDI:: NC_000002.12:5987888:A:G
Gene:: LOC400940 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000002.12:g.5987889A>G, NC_000002.11:g.6128021A>G, NR_026833.1:n.3120A>G

Select item 146926124320.

rs1469261243 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:5986475 (GRCh38)
2:6126607 (GRCh37)
Canonical SPDI:: NC_000002.12:5986474:G:A
Gene:: LOC400940 (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=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.5986475G>A, NC_000002.11:g.6126607G>A, NR_026833.1:n.1706G>A

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