SNP Links for Nucleotide (Select 572153115) - SNP

Links from Nucleotide

Items: 1 to 20 of 122

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Select item 14896265571.

rs1489626557 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:186033571 (GRCh38)
2:186898298 (GRCh37)
Canonical SPDI:: NC_000002.12:186033570:T:C
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000002.12:g.186033571T>C, NC_000002.11:g.186898298T>C, NR_110218.1:n.565A>G

Select item 14822507942.

rs1482250794 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:186033627 (GRCh38)
2:186898354 (GRCh37)
Canonical SPDI:: NC_000002.12:186033626:A:G
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000021/3 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000002.12:g.186033627A>G, NC_000002.11:g.186898354A>G, NR_110218.1:n.509T>C

Select item 14804192903.

rs1480419290 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 2:186083180 (GRCh38)
2:186947907 (GRCh37)
Canonical SPDI:: NC_000002.12:186083179:C:A,NC_000002.12:186083179:C:T
Gene:: LINC01473 (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=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.186083180C>A, NC_000002.12:g.186083180C>T, NC_000002.11:g.186947907C>A, NC_000002.11:g.186947907C>T, NR_110218.1:n.59G>T, NR_110218.1:n.59G>A

Select item 14754011934.

rs1475401193 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:186033574 (GRCh38)
2:186898301 (GRCh37)
Canonical SPDI:: NC_000002.12:186033573:A:G
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.186033574A>G, NC_000002.11:g.186898301A>G, NR_110218.1:n.562T>C

Select item 14670231035.

rs1467023103 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:186038381 (GRCh38)
2:186903108 (GRCh37)
Canonical SPDI:: NC_000002.12:186038380:G:A,NC_000002.12:186038380:G:T
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000002.12:g.186038381G>A, NC_000002.12:g.186038381G>T, NC_000002.11:g.186903108G>A, NC_000002.11:g.186903108G>T, NR_110218.1:n.283C>T, NR_110218.1:n.283C>A

Select item 14655930386.

rs1465593038 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 2:186038392 (GRCh38)
2:186903119 (GRCh37)
Canonical SPDI:: NC_000002.12:186038391:T:A
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000002.12:g.186038392T>A, NC_000002.11:g.186903119T>A, NR_110218.1:n.272A>T

Select item 14558334637.

rs1455833463 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:186033774 (GRCh38)
2:186898501 (GRCh37)
Canonical SPDI:: NC_000002.12:186033773:G:C
Gene:: LINC01473 (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_000002.12:g.186033774G>C, NC_000002.11:g.186898501G>C, NR_110218.1:n.362C>G

Select item 14548288558.

rs1454828855 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:186038409 (GRCh38)
2:186903136 (GRCh37)
Canonical SPDI:: NC_000002.12:186038408:T:G
Gene:: LINC01473 (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.186038409T>G, NC_000002.11:g.186903136T>G, NR_110218.1:n.255A>C

Select item 14438207879.

rs1443820787 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:186081370 (GRCh38)
2:186946097 (GRCh37)
Canonical SPDI:: NC_000002.12:186081369:T:C
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.186081370T>C, NC_000002.11:g.186946097T>C, NR_110218.1:n.132A>G

Select item 144110416710.

rs1441104167 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:186038349 (GRCh38)
2:186903076 (GRCh37)
Canonical SPDI:: NC_000002.12:186038348:T:G
Gene:: LINC01473 (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.186038349T>G, NC_000002.11:g.186903076T>G, NR_110218.1:n.315A>C

Select item 143499434311.

rs1434994343 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:186033623 (GRCh38)
2:186898350 (GRCh37)
Canonical SPDI:: NC_000002.12:186033622:G:A,NC_000002.12:186033622:G:C
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.186033623G>A, NC_000002.12:g.186033623G>C, NC_000002.11:g.186898350G>A, NC_000002.11:g.186898350G>C, NR_110218.1:n.513C>T, NR_110218.1:n.513C>G

Select item 142785536212.

rs1427855362 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 2:186083203 (GRCh38)
2:186947930 (GRCh37)
Canonical SPDI:: NC_000002.12:186083202:T:A,NC_000002.12:186083202:T:C
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.186083203T>A, NC_000002.12:g.186083203T>C, NC_000002.11:g.186947930T>A, NC_000002.11:g.186947930T>C, NR_110218.1:n.36A>T, NR_110218.1:n.36A>G

Select item 142361324713.

rs1423613247 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:186033717 (GRCh38)
2:186898444 (GRCh37)
Canonical SPDI:: NC_000002.12:186033716:T:C
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.186033717T>C, NC_000002.11:g.186898444T>C, NR_110218.1:n.419A>G

Select item 141464933314.

rs1414649333 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:186033711 (GRCh38)
2:186898438 (GRCh37)
Canonical SPDI:: NC_000002.12:186033710:G:T
Gene:: LINC01473 (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_000002.12:g.186033711G>T, NC_000002.11:g.186898438G>T, NR_110218.1:n.425C>A

Select item 139536776315.

rs1395367763 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:186033690 (GRCh38)
2:186898417 (GRCh37)
Canonical SPDI:: NC_000002.12:186033689:T:C
Gene:: LINC01473 (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=0.000023/6 (TOPMED)
HGVS:: NC_000002.12:g.186033690T>C, NC_000002.11:g.186898417T>C, NR_110218.1:n.446A>G

Select item 139103691416.

rs1391036914 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:186033784 (GRCh38)
2:186898511 (GRCh37)
Canonical SPDI:: NC_000002.12:186033783:A:G
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.186033784A>G, NC_000002.11:g.186898511A>G, NR_110218.1:n.352T>C

Select item 138353468517.

rs1383534685 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 2:186033613 (GRCh38)
2:186898340 (GRCh37)
Canonical SPDI:: NC_000002.12:186033612:T:C,NC_000002.12:186033612:T:G
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.186033613T>C, NC_000002.12:g.186033613T>G, NC_000002.11:g.186898340T>C, NC_000002.11:g.186898340T>G, NR_110218.1:n.523A>G, NR_110218.1:n.523A>C

Select item 137605743918.

rs1376057439 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:186038394 (GRCh38)
2:186903121 (GRCh37)
Canonical SPDI:: NC_000002.12:186038393:A:C
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.186038394A>C, NC_000002.11:g.186903121A>C, NR_110218.1:n.270T>G

Select item 137571357119.

rs1375713571 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:186038352 (GRCh38)
2:186903079 (GRCh37)
Canonical SPDI:: NC_000002.12:186038351:A:G
Gene:: LINC01473 (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.186038352A>G, NC_000002.11:g.186903079A>G, NR_110218.1:n.312T>C

Select item 137167866720.

rs1371678667 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 2:186083187 (GRCh38)
2:186947914 (GRCh37)
Canonical SPDI:: NC_000002.12:186083186:A:
Gene:: LINC01473 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.0002/1 (ALFA)
-=0.0002/1 (Estonian)
HGVS:: NC_000002.12:g.186083187del, NC_000002.11:g.186947914del, NR_110218.1:n.52del

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