SNP Links for Nucleotide (Select 564730714) - SNP

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Links from Nucleotide

Items: 1 to 20 of 461

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Select item 14906830121.

rs1490683012 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:20742723 (GRCh38)
21:22115041 (GRCh37)
Canonical SPDI:: NC_000021.9:20742722:G:A
Gene:: LINC00320 (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_000021.9:g.20742723G>A, NC_000021.8:g.22115041G>A, NR_024090.2:n.1886C>T, NR_024090.1:n.1886C>T, NR_109786.1:n.1997C>T, NR_109788.1:n.1823C>T, NR_109787.1:n.1762C>T

Select item 14898697542.

rs1489869754 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:20743814 (GRCh38)
21:22116132 (GRCh37)
Canonical SPDI:: NC_000021.9:20743813:T:C
Gene:: LINC00320 (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=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.20743814T>C, NC_000021.8:g.22116132T>C, NR_024090.2:n.795A>G, NR_024090.1:n.795A>G, NR_109786.1:n.906A>G, NR_109788.1:n.732A>G, NR_109787.1:n.671A>G

Select item 14893514563.

rs1489351456 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:20803024 (GRCh38)
21:22175342 (GRCh37)
Canonical SPDI:: NC_000021.9:20803023:C:T
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000021.9:g.20803024C>T, NC_000021.8:g.22175342C>T, NR_024090.2:n.85G>A, NR_024090.1:n.85G>A, NR_109786.1:n.85G>A, NR_109788.1:n.85G>A, NR_109787.1:n.85G>A

Select item 14854099654.

rs1485409965 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:20743787 (GRCh38)
21:22116105 (GRCh37)
Canonical SPDI:: NC_000021.9:20743786:A:G
Gene:: LINC00320 (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_000021.9:g.20743787A>G, NC_000021.8:g.22116105A>G, NR_024090.2:n.822T>C, NR_024090.1:n.822T>C, NR_109786.1:n.933T>C, NR_109788.1:n.759T>C, NR_109787.1:n.698T>C

Select item 14840055215.

rs1484005521 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:20743646 (GRCh38)
21:22115964 (GRCh37)
Canonical SPDI:: NC_000021.9:20743645:A:G
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.20743646A>G, NC_000021.8:g.22115964A>G, NR_024090.2:n.963T>C, NR_024090.1:n.963T>C, NR_109786.1:n.1074T>C, NR_109788.1:n.900T>C, NR_109787.1:n.839T>C

Select item 14830884466.

rs1483088446 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 21:20781429 (GRCh38)
21:22153747 (GRCh37)
Canonical SPDI:: NC_000021.9:20781428:T:G
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0.0002/1 (ALFA)
G=0.0002/1 (Estonian)
HGVS:: NC_000021.9:g.20781429T>G, NC_000021.8:g.22153747T>G, NR_024090.2:n.445A>C, NR_024090.1:n.445A>C, NR_109786.1:n.449A>C, NR_109788.1:n.502A>C, NR_109787.1:n.441A>C

Select item 14767931227.

rs1476793122 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:20742821 (GRCh38)
21:22115139 (GRCh37)
Canonical SPDI:: NC_000021.9:20742820:A:G
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.20742821A>G, NC_000021.8:g.22115139A>G, NR_024090.2:n.1788T>C, NR_024090.1:n.1788T>C, NR_109786.1:n.1899T>C, NR_109788.1:n.1725T>C, NR_109787.1:n.1664T>C

Select item 14765908338.

rs1476590833 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:20782344 (GRCh38)
21:22154662 (GRCh37)
Canonical SPDI:: NC_000021.9:20782343:C:T
Gene:: LINC00320 (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_000021.9:g.20782344C>T, NC_000021.8:g.22154662C>T, NR_024090.2:n.270G>A, NR_024090.1:n.270G>A, NR_109786.1:n.217G>A, NR_109788.1:n.270G>A, NR_109787.1:n.266G>A

Select item 14764623619.

rs1476462361 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:20743050 (GRCh38)
21:22115368 (GRCh37)
Canonical SPDI:: NC_000021.9:20743049:T:C
Gene:: LINC00320 (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_000021.9:g.20743050T>C, NC_000021.8:g.22115368T>C, NR_024090.2:n.1559A>G, NR_024090.1:n.1559A>G, NR_109786.1:n.1670A>G, NR_109788.1:n.1496A>G, NR_109787.1:n.1435A>G

Select item 147625871510.

rs1476258715 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 21:20782313 (GRCh38)
21:22154631 (GRCh37)
Canonical SPDI:: NC_000021.9:20782312:C:A,NC_000021.9:20782312:C:T
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.20782313C>A, NC_000021.9:g.20782313C>T, NC_000021.8:g.22154631C>A, NC_000021.8:g.22154631C>T, NR_024090.2:n.301G>T, NR_024090.2:n.301G>A, NR_024090.1:n.301G>T, NR_024090.1:n.301G>A, NR_109786.1:n.248G>T, NR_109786.1:n.248G>A, NR_109788.1:n.301G>T, NR_109788.1:n.301G>A, NR_109787.1:n.297G>T, NR_109787.1:n.297G>A

Select item 147447222711.

rs1474472227 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 21:20743277 (GRCh38)
21:22115595 (GRCh37)
Canonical SPDI:: NC_000021.9:20743276:T:C,NC_000021.9:20743276:T:G
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000034/9 (TOPMED)
HGVS:: NC_000021.9:g.20743277T>C, NC_000021.9:g.20743277T>G, NC_000021.8:g.22115595T>C, NC_000021.8:g.22115595T>G, NR_024090.2:n.1332A>G, NR_024090.2:n.1332A>C, NR_024090.1:n.1332A>G, NR_024090.1:n.1332A>C, NR_109786.1:n.1443A>G, NR_109786.1:n.1443A>C, NR_109788.1:n.1269A>G, NR_109788.1:n.1269A>C, NR_109787.1:n.1208A>G, NR_109787.1:n.1208A>C

Select item 147353144212.

rs1473531442 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 21:20743757 (GRCh38)
21:22116075 (GRCh37)
Canonical SPDI:: NC_000021.9:20743756:A:C,NC_000021.9:20743756:A:G
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000021.9:g.20743757A>C, NC_000021.9:g.20743757A>G, NC_000021.8:g.22116075A>C, NC_000021.8:g.22116075A>G, NR_024090.2:n.852T>G, NR_024090.2:n.852T>C, NR_024090.1:n.852T>G, NR_024090.1:n.852T>C, NR_109786.1:n.963T>G, NR_109786.1:n.963T>C, NR_109788.1:n.789T>G, NR_109788.1:n.789T>C, NR_109787.1:n.728T>G, NR_109787.1:n.728T>C

Select item 147117660713.

rs1471176607 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:20743384 (GRCh38)
21:22115702 (GRCh37)
Canonical SPDI:: NC_000021.9:20743383:T:C
Gene:: LINC00320 (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=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.20743384T>C, NC_000021.8:g.22115702T>C, NR_024090.2:n.1225A>G, NR_024090.1:n.1225A>G, NR_109786.1:n.1336A>G, NR_109788.1:n.1162A>G, NR_109787.1:n.1101A>G

Select item 147097782614.

rs1470977826 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:20742833 (GRCh38)
21:22115151 (GRCh37)
Canonical SPDI:: NC_000021.9:20742832:T:C
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
HGVS:: NC_000021.9:g.20742833T>C, NC_000021.8:g.22115151T>C, NR_024090.2:n.1776A>G, NR_024090.1:n.1776A>G, NR_109786.1:n.1887A>G, NR_109788.1:n.1713A>G, NR_109787.1:n.1652A>G

Select item 146909334615.

rs1469093346 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:20743058 (GRCh38)
21:22115376 (GRCh37)
Canonical SPDI:: NC_000021.9:20743057:T:C
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000021.9:g.20743058T>C, NC_000021.8:g.22115376T>C, NR_024090.2:n.1551A>G, NR_024090.1:n.1551A>G, NR_109786.1:n.1662A>G, NR_109788.1:n.1488A>G, NR_109787.1:n.1427A>G

Select item 146830424616.

rs1468304246 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 21:20743747 (GRCh38)
21:22116065 (GRCh37)
Canonical SPDI:: NC_000021.9:20743746:C:A
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00003/8 (TOPMED)
A=0.000057/8 (GnomAD)
HGVS:: NC_000021.9:g.20743747C>A, NC_000021.8:g.22116065C>A, NR_024090.2:n.862G>T, NR_024090.1:n.862G>T, NR_109786.1:n.973G>T, NR_109788.1:n.799G>T, NR_109787.1:n.738G>T

Select item 146776953717.

rs1467769537 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:20743499 (GRCh38)
21:22115817 (GRCh37)
Canonical SPDI:: NC_000021.9:20743498:C:T
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.20743499C>T, NC_000021.8:g.22115817C>T, NR_024090.2:n.1110G>A, NR_024090.1:n.1110G>A, NR_109786.1:n.1221G>A, NR_109788.1:n.1047G>A, NR_109787.1:n.986G>A

Select item 146436672218.

rs1464366722 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:20778418 (GRCh38)
21:22150736 (GRCh37)
Canonical SPDI:: NC_000021.9:20778417:A:G
Gene:: LINC00320 (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=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.20778418A>G, NC_000021.8:g.22150736A>G, NR_024090.2:n.775T>C, NR_024090.1:n.775T>C, NR_109786.1:n.779T>C, NR_109788.1:n.712T>C, NR_109787.1:n.651T>C

Select item 146422862319.

rs1464228623 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 21:20782338 (GRCh38)
21:22154656 (GRCh37)
Canonical SPDI:: NC_000021.9:20782337:G:C
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.20782338G>C, NC_000021.8:g.22154656G>C, NR_024090.2:n.276C>G, NR_024090.1:n.276C>G, NR_109786.1:n.223C>G, NR_109788.1:n.276C>G, NR_109787.1:n.272C>G

Select item 146181802620.

rs1461818026 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 21:20742917 (GRCh38)
21:22115235 (GRCh37)
Canonical SPDI:: NC_000021.9:20742916:A:T
Gene:: LINC00320 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.20742917A>T, NC_000021.8:g.22115235A>T, NR_024090.2:n.1692T>A, NR_024090.1:n.1692T>A, NR_109786.1:n.1803T>A, NR_109788.1:n.1629T>A, NR_109787.1:n.1568T>A

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