SNP Links for Gene (Select 100507073) - SNP

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Select item 14915685021.

rs1491568502 has merged into rs36043717 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 2:66685828 (GRCh38)
2:66912960 (GRCh37)
Canonical SPDI:: NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000002.12:66685816:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
TT=0.471446/2361 (1000Genomes)
HGVS:: NC_000002.12:g.66685828_66685838del, NC_000002.12:g.66685830_66685838del, NC_000002.12:g.66685832_66685838del, NC_000002.12:g.66685833_66685838del, NC_000002.12:g.66685834_66685838del, NC_000002.12:g.66685835_66685838del, NC_000002.12:g.66685836_66685838del, NC_000002.12:g.66685837_66685838del, NC_000002.12:g.66685838del, NC_000002.12:g.66685838dup, NC_000002.12:g.66685837_66685838dup, NC_000002.12:g.66685836_66685838dup, NC_000002.12:g.66685835_66685838dup, NC_000002.12:g.66685834_66685838dup, NC_000002.12:g.66685833_66685838dup, NC_000002.12:g.66685832_66685838dup, NC_000002.12:g.66685831_66685838dup, NC_000002.12:g.66685830_66685838dup, NC_000002.12:g.66685829_66685838dup, NC_000002.12:g.66685828_66685838dup, NC_000002.11:g.66912960_66912970del, NC_000002.11:g.66912962_66912970del, NC_000002.11:g.66912964_66912970del, NC_000002.11:g.66912965_66912970del, NC_000002.11:g.66912966_66912970del, NC_000002.11:g.66912967_66912970del, NC_000002.11:g.66912968_66912970del, NC_000002.11:g.66912969_66912970del, NC_000002.11:g.66912970del, NC_000002.11:g.66912970dup, NC_000002.11:g.66912969_66912970dup, NC_000002.11:g.66912968_66912970dup, NC_000002.11:g.66912967_66912970dup, NC_000002.11:g.66912966_66912970dup, NC_000002.11:g.66912965_66912970dup, NC_000002.11:g.66912964_66912970dup, NC_000002.11:g.66912963_66912970dup, NC_000002.11:g.66912962_66912970dup, NC_000002.11:g.66912961_66912970dup, NC_000002.11:g.66912960_66912970dup

Select item 14915152482.

rs1491515248 has merged into rs1228826708 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGGGGGGG>-,G,GG,GGG,GGGG,GGGGG,GGGGGG,GGGGGGG,GGGGGGGGG,GGGGGGGGGG,GGGGGGGGGGG [Show Flanks]
Chromosome:: 2:66574432 (GRCh38)
2:66801564 (GRCh37)
Canonical SPDI:: NC_000002.12:66574429:GGGGGGGGGG:GG,NC_000002.12:66574429:GGGGGGGGGG:GGG,NC_000002.12:66574429:GGGGGGGGGG:GGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGGGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGGGGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGGGGGGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGGGGGGGGG,NC_000002.12:66574429:GGGGGGGGGG:GGGGGGGGGGGGG
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
HGVS:: NC_000002.12:g.66574432_66574439del, NC_000002.12:g.66574433_66574439del, NC_000002.12:g.66574434_66574439del, NC_000002.12:g.66574435_66574439del, NC_000002.12:g.66574436_66574439del, NC_000002.12:g.66574437_66574439del, NC_000002.12:g.66574438_66574439del, NC_000002.12:g.66574439del, NC_000002.12:g.66574439dup, NC_000002.12:g.66574438_66574439dup, NC_000002.12:g.66574437_66574439dup, NC_000002.11:g.66801564_66801571del, NC_000002.11:g.66801565_66801571del, NC_000002.11:g.66801566_66801571del, NC_000002.11:g.66801567_66801571del, NC_000002.11:g.66801568_66801571del, NC_000002.11:g.66801569_66801571del, NC_000002.11:g.66801570_66801571del, NC_000002.11:g.66801571del, NC_000002.11:g.66801571dup, NC_000002.11:g.66801570_66801571dup, NC_000002.11:g.66801569_66801571dup, NG_011467.1:g.144033_144040del, NG_011467.1:g.144034_144040del, NG_011467.1:g.144035_144040del, NG_011467.1:g.144036_144040del, NG_011467.1:g.144037_144040del, NG_011467.1:g.144038_144040del, NG_011467.1:g.144039_144040del, NG_011467.1:g.144040del, NG_011467.1:g.144040dup, NG_011467.1:g.144039_144040dup, NG_011467.1:g.144038_144040dup

Select item 14913927093.

rs1491392709 has merged into rs5831826 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: 2:66593643 (GRCh38)
2:66820775 (GRCh37)
Canonical SPDI:: NC_000002.12:66593632:TTTTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:66593632:TTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:66593632:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:66593632:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:66593632:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:66593632:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000002.12:66593632:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.2012/746 (TWINSUK)
T=0.2034/784 (ALSPAC)
T=0.325/13 (GENOME_DK)
HGVS:: NC_000002.12:g.66593643_66593646del, NC_000002.12:g.66593644_66593646del, NC_000002.12:g.66593645_66593646del, NC_000002.12:g.66593646del, NC_000002.12:g.66593646dup, NC_000002.12:g.66593645_66593646dup, NC_000002.12:g.66593641_66593646dup, NC_000002.11:g.66820775_66820778del, NC_000002.11:g.66820776_66820778del, NC_000002.11:g.66820777_66820778del, NC_000002.11:g.66820778del, NC_000002.11:g.66820778dup, NC_000002.11:g.66820777_66820778dup, NC_000002.11:g.66820773_66820778dup

Select item 14913270974.

rs1491327097 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 2:66579055 (GRCh38)
2:66806187 (GRCh37)
Canonical SPDI:: NC_000002.12:66579054:TC:
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000002.12:g.66579055_66579056del, NC_000002.11:g.66806187_66806188del, NG_055605.1:g.4381_4382del

Select item 14913154625.

rs1491315462 has merged into rs10569711 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATATA>-,TA,TATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA [Show Flanks]
Chromosome:: 2:66602275 (GRCh38)
2:66829407 (GRCh37)
Canonical SPDI:: NC_000002.12:66602263:ATATATATATATATATA:ATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATA,NC_000002.12:66602263:ATATATATATATATATA:ATATATATATATATATATATATATATATA
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATATATATATATA=0./0 (ALFA)
AT=0.194444/7 (GENOME_DK)
AT=0.415358/109941 (TOPMED)
HGVS:: NC_000002.12:g.66602265TA[5], NC_000002.12:g.66602265TA[6], NC_000002.12:g.66602265TA[7], NC_000002.12:g.66602265TA[9], NC_000002.12:g.66602265TA[10], NC_000002.12:g.66602265TA[11], NC_000002.12:g.66602265TA[12], NC_000002.12:g.66602265TA[13], NC_000002.12:g.66602265TA[14], NC_000002.11:g.66829397TA[5], NC_000002.11:g.66829397TA[6], NC_000002.11:g.66829397TA[7], NC_000002.11:g.66829397TA[9], NC_000002.11:g.66829397TA[10], NC_000002.11:g.66829397TA[11], NC_000002.11:g.66829397TA[12], NC_000002.11:g.66829397TA[13], NC_000002.11:g.66829397TA[14]

Select item 14912931946.

rs1491293194 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,C [Show Flanks]
Chromosome:: 2:66685817 (GRCh38)
2:66912950 (GRCh37)
Canonical SPDI:: NC_000002.12:66685817::A,NC_000002.12:66685817::ATA,NC_000002.12:66685817::ATATA,NC_000002.12:66685817::C
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
ATA=0.00033/20 (GnomAD)
A=0.0365/603 (TOMMO)
HGVS:: NC_000002.12:g.66685817_66685818insA, NC_000002.12:g.66685817_66685818insATA, NC_000002.12:g.66685817_66685818insATATA, NC_000002.12:g.66685817_66685818insC, NC_000002.11:g.66912949_66912950insA, NC_000002.11:g.66912949_66912950insATA, NC_000002.11:g.66912949_66912950insATATA, NC_000002.11:g.66912949_66912950insC

Select item 14911929587.

rs1491192958 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 2:66639600 (GRCh38)
2:66866732 (GRCh37)
Canonical SPDI:: NC_000002.12:66639597:TATA:TA
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATA=0.00392/64 (ALFA)
-=0.0025/16 (1000Genomes)
-=0.00333/2 (NorthernSweden)
-=0.00647/602 (GnomAD)
HGVS:: NC_000002.12:g.66639598TA[1], NC_000002.11:g.66866730TA[1]

Select item 14911177868.

rs1491117786 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTT [Show Flanks]
Chromosome:: 2:66593633 (GRCh38)
2:66820766 (GRCh37)
Canonical SPDI:: NC_000002.12:66593633:TTT:TTTGTTT
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTTGTTT=0./0 (ALFA)
TTTG=0.00033/4 (GnomAD)
HGVS:: NC_000002.12:g.66593636_66593637insGTTT, NC_000002.11:g.66820768_66820769insGTTT

Select item 14910590159.

rs1491059015 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 2:66580608 (GRCh38)
2:66807740 (GRCh37)
Canonical SPDI:: NC_000002.12:66580607:TT:
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.66580608_66580609del, NC_000002.11:g.66807740_66807741del

Select item 149104773210.

rs1491047732 has merged into rs70947313 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,TT,TTT,TTTTT,TTTTTT,TTTTTTTT [Show Flanks]
Chromosome:: 2:66648777 (GRCh38)
2:66875909 (GRCh37)
Canonical SPDI:: NC_000002.12:66648767:TTTTTTTTTTTTT:TTTTTTTTT,NC_000002.12:66648767:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:66648767:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000002.12:66648767:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:66648767:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000002.12:66648767:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.4261/1785 (1000Genomes)
HGVS:: NC_000002.12:g.66648777_66648780del, NC_000002.12:g.66648779_66648780del, NC_000002.12:g.66648780del, NC_000002.12:g.66648780dup, NC_000002.12:g.66648779_66648780dup, NC_000002.12:g.66648777_66648780dup, NC_000002.11:g.66875909_66875912del, NC_000002.11:g.66875911_66875912del, NC_000002.11:g.66875912del, NC_000002.11:g.66875912dup, NC_000002.11:g.66875911_66875912dup, NC_000002.11:g.66875909_66875912dup

Select item 149102963411.

rs1491029634 has merged into rs111729742 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT [Show Flanks]
Chromosome:: 2:66579054 (GRCh38)
2:66806186 (GRCh37)
Canonical SPDI:: NC_000002.12:66579043:TTTTTTTTTTTT:TTTTTTTTTT,NC_000002.12:66579043:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000002.12:66579043:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000002.12:66579043:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000002.12:66579043:TTTTTTTTTTTT:TTTTTTTTTTTTTTT
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
T=0.1871/937 (1000Genomes)
HGVS:: NC_000002.12:g.66579054_66579055del, NC_000002.12:g.66579055del, NC_000002.12:g.66579055dup, NC_000002.12:g.66579054_66579055dup, NC_000002.12:g.66579053_66579055dup, NC_000002.11:g.66806186_66806187del, NC_000002.11:g.66806187del, NC_000002.11:g.66806187dup, NC_000002.11:g.66806186_66806187dup, NC_000002.11:g.66806185_66806187dup, NG_055605.1:g.4380_4381del, NG_055605.1:g.4381del, NG_055605.1:g.4381dup, NG_055605.1:g.4380_4381dup, NG_055605.1:g.4379_4381dup

Select item 149098689612.

rs1490986896 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:66663073 (GRCh38)
2:66890205 (GRCh37)
Canonical SPDI:: NC_000002.12:66663072:T:C
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_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.66663073T>C, NC_000002.11:g.66890205T>C

Select item 149098155213.

rs1490981552 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGT>- [Show Flanks]
Chromosome:: 2:66662948 (GRCh38)
2:66890080 (GRCh37)
Canonical SPDI:: NC_000002.12:66662946:TATATATATATATATATATATATATATATATATATATGTGTGTGTGTGTGT:T
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.00019/10 (GnomAD)
HGVS:: NC_000002.12:g.66662948_66662997del, NC_000002.11:g.66890080_66890129del

Select item 149097199514.

rs1490971995 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 2:66596181 (GRCh38)
2:66823313 (GRCh37)
Canonical SPDI:: NC_000002.12:66596180:C:G,NC_000002.12:66596180:C:T
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.003245/53 (ALFA)
G=0.000008/1 (GnomAD)
HGVS:: NC_000002.12:g.66596181C>G, NC_000002.12:g.66596181C>T, NC_000002.11:g.66823313C>G, NC_000002.11:g.66823313C>T

Select item 149094338315.

rs1490943383 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:66648594 (GRCh38)
2:66875726 (GRCh37)
Canonical SPDI:: NC_000002.12:66648593:C:G
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.66648594C>G, NC_000002.11:g.66875726C>G

Select item 149091693216.

rs1490916932 [Homo sapiens]

Variant type:: SNV:
Alleles:: GT>-
Chromosome:: no mapping
Canonical SPDI:

Select item 149091286817.

rs1490912868 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:66679331 (GRCh38)
2:66906463 (GRCh37)
Canonical SPDI:: NC_000002.12:66679330:G:A
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_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.66679331G>A, NC_000002.11:g.66906463G>A

Select item 149089708318.

rs1490897083 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:66679466 (GRCh38)
2:66906598 (GRCh37)
Canonical SPDI:: NC_000002.12:66679465:G:C
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000002.12:g.66679466G>C, NC_000002.11:g.66906598G>C

Select item 149088502719.

rs1490885027 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 2:66648565 (GRCh38)
2:66875697 (GRCh37)
Canonical SPDI:: NC_000002.12:66648564:T:C,NC_000002.12:66648564:T:G
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.66648565T>C, NC_000002.12:g.66648565T>G, NC_000002.11:g.66875697T>C, NC_000002.11:g.66875697T>G

Select item 149086271920.

rs1490862719 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:66693201 (GRCh38)
2:66920333 (GRCh37)
Canonical SPDI:: NC_000002.12:66693200:A:G
Gene:: LINC01798 (Varview)
Functional Consequence:: intron_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.66693201A>G, NC_000002.11:g.66920333A>G

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