SNP Links for Nucleotide (Select 723428431) - SNP

Links from Nucleotide

Items: 1 to 20 of 154

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Select item 14837019051.

rs1483701905 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:60057359 (GRCh38)
20:58632414 (GRCh37)
Canonical SPDI:: NC_000020.11:60057358:G:A
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.60057359G>A, NC_000020.10:g.58632414G>A, NR_126504.1:n.114G>A

Select item 14725774492.

rs1472577449 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:60057571 (GRCh38)
20:58632626 (GRCh37)
Canonical SPDI:: NC_000020.11:60057570:G:A
Gene:: LINC02910 (Varview)
Functional Consequence:: intron_variant,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_000020.11:g.60057571G>A, NC_000020.10:g.58632626G>A, NR_126504.1:n.326G>A

Select item 14569949473.

rs1456994947 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:60057343 (GRCh38)
20:58632398 (GRCh37)
Canonical SPDI:: NC_000020.11:60057342:T:C
Gene:: LINC02910 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000020.11:g.60057343T>C, NC_000020.10:g.58632398T>C, NR_126504.1:n.98T>C

Select item 14521974364.

rs1452197436 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:60057685 (GRCh38)
20:58632740 (GRCh37)
Canonical SPDI:: NC_000020.11:60057684:A:G
Gene:: LINC02910 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000020.11:g.60057685A>G, NC_000020.10:g.58632740A>G, NR_126504.1:n.440A>G

Select item 14516276455.

rs1451627645 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 20:60057668 (GRCh38)
20:58632723 (GRCh37)
Canonical SPDI:: NC_000020.11:60057667:G:A,NC_000020.11:60057667:G:T
Gene:: LINC02910 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000020.11:g.60057668G>A, NC_000020.11:g.60057668G>T, NC_000020.10:g.58632723G>A, NC_000020.10:g.58632723G>T, NR_126504.1:n.423G>A, NR_126504.1:n.423G>T

Select item 14510223946.

rs1451022394 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:60057788 (GRCh38)
20:58632843 (GRCh37)
Canonical SPDI:: NC_000020.11:60057787:G:A
Gene:: LINC02910 (Varview)
Functional Consequence:: intron_variant,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_000020.11:g.60057788G>A, NC_000020.10:g.58632843G>A, NR_126504.1:n.543G>A

Select item 14506136497.

rs1450613649 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 20:60055983 (GRCh38)
20:58631038 (GRCh37)
Canonical SPDI:: NC_000020.11:60055982:C:G,NC_000020.11:60055982:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000020.11:g.60055983C>G, NC_000020.11:g.60055983C>T, NC_000020.10:g.58631038C>G, NC_000020.10:g.58631038C>T, NM_173644.2:c.-248C>G, NM_173644.2:c.-248C>T, NR_161291.1:n.59C>G, NR_161291.1:n.59C>T, NM_173644.1:c.-248C>G, NM_173644.1:c.-248C>T, NR_161292.1:n.59C>G, NR_161292.1:n.59C>T, NM_001302813.1:c.-168C>G, NM_001302813.1:c.-168C>T, NR_161293.1:n.59C>G, NR_161293.1:n.59C>T, NM_001302815.1:c.-248C>G, NM_001302815.1:c.-248C>T, NR_126504.1:n.59C>G, NR_126504.1:n.59C>T

Select item 14371667658.

rs1437166765 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:60057887 (GRCh38)
20:58632942 (GRCh37)
Canonical SPDI:: NC_000020.11:60057886:T:C
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000020.11:g.60057887T>C, NC_000020.10:g.58632942T>C, NR_126504.1:n.642T>C

Select item 14233604759.

rs1423360475 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:60057399 (GRCh38)
20:58632454 (GRCh37)
Canonical SPDI:: NC_000020.11:60057398:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
HGVS:: NC_000020.11:g.60057399C>T, NC_000020.10:g.58632454C>T, NR_126504.1:n.154C>T

Select item 141668130210.

rs1416681302 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:60057671 (GRCh38)
20:58632726 (GRCh37)
Canonical SPDI:: NC_000020.11:60057670:T:C
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.60057671T>C, NC_000020.10:g.58632726T>C, NR_126504.1:n.426T>C

Select item 141531012811.

rs1415310128 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:60057871 (GRCh38)
20:58632926 (GRCh37)
Canonical SPDI:: NC_000020.11:60057870:G:A
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000020.11:g.60057871G>A, NC_000020.10:g.58632926G>A, NR_126504.1:n.626G>A

Select item 141148500912.

rs1411485009 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:60056006 (GRCh38)
20:58631061 (GRCh37)
Canonical SPDI:: NC_000020.11:60056005:G:A
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000020.11:g.60056006G>A, NC_000020.10:g.58631061G>A, NM_173644.2:c.-225G>A, NR_161291.1:n.82G>A, NM_173644.1:c.-225G>A, NR_161292.1:n.82G>A, NM_001302813.1:c.-145G>A, NR_161293.1:n.82G>A, NM_001302815.1:c.-225G>A, NR_126504.1:n.82G>A

Select item 140930059413.

rs1409300594 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 20:60057603 (GRCh38)
20:58632658 (GRCh37)
Canonical SPDI:: NC_000020.11:60057602:C:A,NC_000020.11:60057602:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000021/3 (GnomAD)
T=0.00003/8 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000020.11:g.60057603C>A, NC_000020.11:g.60057603C>T, NC_000020.10:g.58632658C>A, NC_000020.10:g.58632658C>T, NR_126504.1:n.358C>A, NR_126504.1:n.358C>T

Select item 140907957414.

rs1409079574 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:60057562 (GRCh38)
20:58632617 (GRCh37)
Canonical SPDI:: NC_000020.11:60057561:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.60057562C>T, NC_000020.10:g.58632617C>T, NR_126504.1:n.317C>T

Select item 140477460115.

rs1404774601 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:60056007 (GRCh38)
20:58631062 (GRCh37)
Canonical SPDI:: NC_000020.11:60056006:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (KOREAN)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.60056007C>T, NC_000020.10:g.58631062C>T, NM_173644.2:c.-224C>T, NR_161291.1:n.83C>T, NM_173644.1:c.-224C>T, NR_161292.1:n.83C>T, NM_001302813.1:c.-144C>T, NR_161293.1:n.83C>T, NM_001302815.1:c.-224C>T, NR_126504.1:n.83C>T

Select item 138856986616.

rs1388569866 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:60057758 (GRCh38)
20:58632813 (GRCh37)
Canonical SPDI:: NC_000020.11:60057757:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.60057758C>T, NC_000020.10:g.58632813C>T, NR_126504.1:n.513C>T

Select item 138600286817.

rs1386002868 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:60057336 (GRCh38)
20:58632391 (GRCh37)
Canonical SPDI:: NC_000020.11:60057335:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000029/4 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000020.11:g.60057336C>T, NC_000020.10:g.58632391C>T, NR_126504.1:n.91C>T

Select item 138595854918.

rs1385958549 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:60057638 (GRCh38)
20:58632693 (GRCh37)
Canonical SPDI:: NC_000020.11:60057637:G:A
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000020.11:g.60057638G>A, NC_000020.10:g.58632693G>A, NR_126504.1:n.393G>A

Select item 137579809019.

rs1375798090 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:60057438 (GRCh38)
20:58632493 (GRCh37)
Canonical SPDI:: NC_000020.11:60057437:C:T
Gene:: LINC02910 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000020.11:g.60057438C>T, NC_000020.10:g.58632493C>T, NR_126504.1:n.193C>T

Select item 136953439320.

rs1369534393 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:60057572 (GRCh38)
20:58632627 (GRCh37)
Canonical SPDI:: NC_000020.11:60057571:G:A
Gene:: LINC02910 (Varview)
Functional Consequence:: intron_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)
HGVS:: NC_000020.11:g.60057572G>A, NC_000020.10:g.58632627G>A, NR_126504.1:n.327G>A

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