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Select item 14915404831.

rs1491540483 [Homo sapiens]

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

Select item 14914170102.

rs1491417010 has merged into rs56084078 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:76620874 (GRCh38)
7:76250191 (GRCh37)
Canonical SPDI:: NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000007.14:g.76620874_76620886del, NC_000007.14:g.76620875_76620886del, NC_000007.14:g.76620876_76620886del, NC_000007.14:g.76620877_76620886del, NC_000007.14:g.76620878_76620886del, NC_000007.14:g.76620879_76620886del, NC_000007.14:g.76620880_76620886del, NC_000007.14:g.76620881_76620886del, NC_000007.14:g.76620882_76620886del, NC_000007.14:g.76620883_76620886del, NC_000007.14:g.76620884_76620886del, NC_000007.14:g.76620885_76620886del, NC_000007.14:g.76620886del, NC_000007.14:g.76620886dup, NC_000007.14:g.76620885_76620886dup, NC_000007.14:g.76620884_76620886dup, NC_000007.14:g.76620883_76620886dup, NC_000007.14:g.76620882_76620886dup, NC_000007.14:g.76620881_76620886dup, NC_000007.14:g.76620880_76620886dup, NC_000007.14:g.76620879_76620886dup, NC_000007.14:g.76620878_76620886dup, NC_000007.14:g.76620877_76620886dup, NC_000007.14:g.76620876_76620886dup, NC_000007.14:g.76620875_76620886dup, NC_000007.14:g.76620874_76620886dup, NC_000007.14:g.76620873_76620886dup, NC_000007.14:g.76620871_76620886dup, NC_000007.14:g.76620870_76620886dup, NC_000007.14:g.76620867_76620886dup, NC_000007.14:g.76620886_76620887insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.76250191_76250203del, NC_000007.13:g.76250192_76250203del, NC_000007.13:g.76250193_76250203del, NC_000007.13:g.76250194_76250203del, NC_000007.13:g.76250195_76250203del, NC_000007.13:g.76250196_76250203del, NC_000007.13:g.76250197_76250203del, NC_000007.13:g.76250198_76250203del, NC_000007.13:g.76250199_76250203del, NC_000007.13:g.76250200_76250203del, NC_000007.13:g.76250201_76250203del, NC_000007.13:g.76250202_76250203del, NC_000007.13:g.76250203del, NC_000007.13:g.76250203dup, NC_000007.13:g.76250202_76250203dup, NC_000007.13:g.76250201_76250203dup, NC_000007.13:g.76250200_76250203dup, NC_000007.13:g.76250199_76250203dup, NC_000007.13:g.76250198_76250203dup, NC_000007.13:g.76250197_76250203dup, NC_000007.13:g.76250196_76250203dup, NC_000007.13:g.76250195_76250203dup, NC_000007.13:g.76250194_76250203dup, NC_000007.13:g.76250193_76250203dup, NC_000007.13:g.76250192_76250203dup, NC_000007.13:g.76250191_76250203dup, NC_000007.13:g.76250190_76250203dup, NC_000007.13:g.76250188_76250203dup, NC_000007.13:g.76250187_76250203dup, NC_000007.13:g.76250184_76250203dup, NC_000007.13:g.76250203_76250204insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187561.1:g.107709_107721del, NT_187561.1:g.107710_107721del, NT_187561.1:g.107711_107721del, NT_187561.1:g.107712_107721del, NT_187561.1:g.107713_107721del, NT_187561.1:g.107714_107721del, NT_187561.1:g.107715_107721del, NT_187561.1:g.107716_107721del, NT_187561.1:g.107717_107721del, NT_187561.1:g.107718_107721del, NT_187561.1:g.107719_107721del, NT_187561.1:g.107720_107721del, NT_187561.1:g.107721del, NT_187561.1:g.107721dup, NT_187561.1:g.107720_107721dup, NT_187561.1:g.107719_107721dup, NT_187561.1:g.107718_107721dup, NT_187561.1:g.107717_107721dup, NT_187561.1:g.107716_107721dup, NT_187561.1:g.107715_107721dup, NT_187561.1:g.107714_107721dup, NT_187561.1:g.107713_107721dup, NT_187561.1:g.107712_107721dup, NT_187561.1:g.107711_107721dup, NT_187561.1:g.107710_107721dup, NT_187561.1:g.107709_107721dup, NT_187561.1:g.107708_107721dup, NT_187561.1:g.107706_107721dup, NT_187561.1:g.107705_107721dup, NT_187561.1:g.107702_107721dup, NT_187561.1:g.107721_107722insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913888433.

rs1491388843 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 7:76620862 (GRCh38)
7:76250180 (GRCh37)
Canonical SPDI:: NC_000007.14:76620862::C
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000007.14:g.76620862_76620863insC, NC_000007.13:g.76250179_76250180insC, NT_187561.1:g.107697_107698insC

Select item 14913527964.

rs1491352796 has merged into rs757086256 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:76622387 (GRCh38)
7:76251704 (GRCh37)
Canonical SPDI:: NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76622374:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
-=0.25/10 (GENOME_DK)
HGVS:: NC_000007.14:g.76622387_76622396del, NC_000007.14:g.76622389_76622396del, NC_000007.14:g.76622390_76622396del, NC_000007.14:g.76622391_76622396del, NC_000007.14:g.76622392_76622396del, NC_000007.14:g.76622393_76622396del, NC_000007.14:g.76622394_76622396del, NC_000007.14:g.76622395_76622396del, NC_000007.14:g.76622396del, NC_000007.14:g.76622396dup, NC_000007.14:g.76622395_76622396dup, NC_000007.14:g.76622394_76622396dup, NC_000007.14:g.76622393_76622396dup, NC_000007.14:g.76622392_76622396dup, NC_000007.14:g.76622391_76622396dup, NC_000007.13:g.76251704_76251713del, NC_000007.13:g.76251706_76251713del, NC_000007.13:g.76251707_76251713del, NC_000007.13:g.76251708_76251713del, NC_000007.13:g.76251709_76251713del, NC_000007.13:g.76251710_76251713del, NC_000007.13:g.76251711_76251713del, NC_000007.13:g.76251712_76251713del, NC_000007.13:g.76251713del, NC_000007.13:g.76251713dup, NC_000007.13:g.76251712_76251713dup, NC_000007.13:g.76251711_76251713dup, NC_000007.13:g.76251710_76251713dup, NC_000007.13:g.76251709_76251713dup, NC_000007.13:g.76251708_76251713dup, NT_187561.1:g.109222_109231del, NT_187561.1:g.109224_109231del, NT_187561.1:g.109225_109231del, NT_187561.1:g.109226_109231del, NT_187561.1:g.109227_109231del, NT_187561.1:g.109228_109231del, NT_187561.1:g.109229_109231del, NT_187561.1:g.109230_109231del, NT_187561.1:g.109231del, NT_187561.1:g.109231dup, NT_187561.1:g.109230_109231dup, NT_187561.1:g.109229_109231dup, NT_187561.1:g.109228_109231dup, NT_187561.1:g.109227_109231dup, NT_187561.1:g.109226_109231dup

Select item 14913312105.

rs1491331210 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 7:76623185 (GRCh38)
7:76252502 (GRCh37)
Canonical SPDI:: NC_000007.14:76623184:GT:
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.002613/31 (ALFA)
-=0.003449/384 (GnomAD)
HGVS:: NC_000007.14:g.76623185_76623186del, NC_000007.13:g.76252502_76252503del, NT_187561.1:g.110020_110021del

Select item 14913018886.

rs1491301888 [Homo sapiens]

Variant type:: INS
Alleles:: ->AAAAAAAAAG,AAAAAAAAG,AAAAAAAG,AAAAG,AAAAGG,AAAG,AAG,AG,AGG [Show Flanks]
Chromosome:: 7:76615989 (GRCh38)
7:76245307 (GRCh37)
Canonical SPDI:: NC_000007.14:76615989::AAAAAAAAAG,NC_000007.14:76615989::AAAAAAAAG,NC_000007.14:76615989::AAAAAAAG,NC_000007.14:76615989::AAAAG,NC_000007.14:76615989::AAAAGG,NC_000007.14:76615989::AAAG,NC_000007.14:76615989::AAG,NC_000007.14:76615989::AG,NC_000007.14:76615989::AGG
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAG=0./0 (ALFA)
HGVS:: NC_000007.14:g.76615989_76615990insAAAAAAAAAG, NC_000007.14:g.76615989_76615990insAAAAAAAAG, NC_000007.14:g.76615989_76615990insAAAAAAAG, NC_000007.14:g.76615989_76615990insAAAAG, NC_000007.14:g.76615989_76615990insAAAAGG, NC_000007.14:g.76615989_76615990insAAAG, NC_000007.14:g.76615989_76615990insAAG, NC_000007.14:g.76615989_76615990insAG, NC_000007.14:g.76615989_76615990insAGG, NC_000007.13:g.76245306_76245307insAAAAAAAAAG, NC_000007.13:g.76245306_76245307insAAAAAAAAG, NC_000007.13:g.76245306_76245307insAAAAAAAG, NC_000007.13:g.76245306_76245307insAAAAG, NC_000007.13:g.76245306_76245307insAAAAGG, NC_000007.13:g.76245306_76245307insAAAG, NC_000007.13:g.76245306_76245307insAAG, NC_000007.13:g.76245306_76245307insAG, NC_000007.13:g.76245306_76245307insAGG, NT_187561.1:g.102824_102825insAAAAAAAAAG, NT_187561.1:g.102824_102825insAAAAAAAAG, NT_187561.1:g.102824_102825insAAAAAAAG, NT_187561.1:g.102824_102825insAAAAG, NT_187561.1:g.102824_102825insAAAAGG, NT_187561.1:g.102824_102825insAAAG, NT_187561.1:g.102824_102825insAAG, NT_187561.1:g.102824_102825insAG, NT_187561.1:g.102824_102825insAGG

Select item 14912717687.

rs1491271768 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGTGGC [Show Flanks]
Chromosome:: 7:76618841 (GRCh38)
7:76248159 (GRCh37)
Canonical SPDI:: NC_000007.14:76618841:CAGTGGC:CAGTGGCAGTGGC
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CAGTGGCAGTGGC=0./0 (ALFA)
HGVS:: NC_000007.14:g.76618843_76618848dup, NC_000007.13:g.76248160_76248165dup, NT_187561.1:g.105678_105683dup

Select item 14912504298.

rs1491250429 has merged into rs1215209887 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TTTT,TTTTTT [Show Flanks]
Chromosome:: 7:76622879 (GRCh38)
7:76252196 (GRCh37)
Canonical SPDI:: NC_000007.14:76622872:TTTTTTTTTTT:TTTTTT,NC_000007.14:76622872:TTTTTTTTTTT:TTTTTTT,NC_000007.14:76622872:TTTTTTTTTTT:TTTTTTTTTT,NC_000007.14:76622872:TTTTTTTTTTT:TTTTTTTTTTTT
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
HGVS:: NC_000007.14:g.76622879_76622883del, NC_000007.14:g.76622880_76622883del, NC_000007.14:g.76622883del, NC_000007.14:g.76622883dup, NC_000007.13:g.76252196_76252200del, NC_000007.13:g.76252197_76252200del, NC_000007.13:g.76252200del, NC_000007.13:g.76252200dup, NT_187561.1:g.109714_109718del, NT_187561.1:g.109715_109718del, NT_187561.1:g.109718del, NT_187561.1:g.109718dup

Select item 14912147239.

rs1491214723 has merged into rs59816962 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAA>-,A,AA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 7:76625141 (GRCh38)
7:76254458 (GRCh37)
Canonical SPDI:: NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000007.14:76625132:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
HGVS:: NC_000007.14:g.76625141_76625152del, NC_000007.14:g.76625142_76625152del, NC_000007.14:g.76625143_76625152del, NC_000007.14:g.76625145_76625152del, NC_000007.14:g.76625147_76625152del, NC_000007.14:g.76625148_76625152del, NC_000007.14:g.76625149_76625152del, NC_000007.14:g.76625150_76625152del, NC_000007.14:g.76625151_76625152del, NC_000007.14:g.76625152del, NC_000007.14:g.76625152dup, NC_000007.14:g.76625151_76625152dup, NC_000007.14:g.76625150_76625152dup, NC_000007.14:g.76625149_76625152dup, NC_000007.14:g.76625148_76625152dup, NC_000007.14:g.76625147_76625152dup, NC_000007.14:g.76625141_76625152dup, NC_000007.13:g.76254458_76254469del, NC_000007.13:g.76254459_76254469del, NC_000007.13:g.76254460_76254469del, NC_000007.13:g.76254462_76254469del, NC_000007.13:g.76254464_76254469del, NC_000007.13:g.76254465_76254469del, NC_000007.13:g.76254466_76254469del, NC_000007.13:g.76254467_76254469del, NC_000007.13:g.76254468_76254469del, NC_000007.13:g.76254469del, NC_000007.13:g.76254469dup, NC_000007.13:g.76254468_76254469dup, NC_000007.13:g.76254467_76254469dup, NC_000007.13:g.76254466_76254469dup, NC_000007.13:g.76254465_76254469dup, NC_000007.13:g.76254464_76254469dup, NC_000007.13:g.76254458_76254469dup, NT_187561.1:g.111976_111987del, NT_187561.1:g.111977_111987del, NT_187561.1:g.111978_111987del, NT_187561.1:g.111980_111987del, NT_187561.1:g.111982_111987del, NT_187561.1:g.111983_111987del, NT_187561.1:g.111984_111987del, NT_187561.1:g.111985_111987del, NT_187561.1:g.111986_111987del, NT_187561.1:g.111987del, NT_187561.1:g.111987dup, NT_187561.1:g.111986_111987dup, NT_187561.1:g.111985_111987dup, NT_187561.1:g.111984_111987dup, NT_187561.1:g.111983_111987dup, NT_187561.1:g.111982_111987dup, NT_187561.1:g.111976_111987dup

Select item 149118235810.

rs1491182358 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:76612394 (GRCh38)
7:76241711 (GRCh37)
Canonical SPDI:: NC_000007.14:76612392:ACA:A
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.76612394_76612395del, NC_000007.13:g.76241711_76241712del, NT_187561.1:g.99229_99230del

Select item 149117609811.

rs1491176098 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 7:76622872 (GRCh38)
7:76252189 (GRCh37)
Canonical SPDI:: NC_000007.14:76622871:CT:
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000036/5 (GnomAD)
HGVS:: NC_000007.14:g.76622872_76622873del, NC_000007.13:g.76252189_76252190del, NT_187561.1:g.109707_109708del

Select item 149115381112.

rs1491153811 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 7:76615989 (GRCh38)
7:76245306 (GRCh37)
Canonical SPDI:: NC_000007.14:76615988:AG:
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01551/184 (ALFA)
-=0.14514/1908 (TOMMO)
HGVS:: NC_000007.14:g.76615989_76615990del, NC_000007.13:g.76245306_76245307del, NT_187561.1:g.102824_102825del

Select item 149113202413.

rs1491132024 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:76625132 (GRCh38)
7:76254449 (GRCh37)
Canonical SPDI:: NC_000007.14:76625131:CA:
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01104/131 (ALFA)
-=0.00117/19 (TOMMO)
HGVS:: NC_000007.14:g.76625132_76625133del, NC_000007.13:g.76254449_76254450del, NT_187561.1:g.111967_111968del

Select item 149100926814.

rs1491009268 has merged into rs71521144 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT [Show Flanks]
Chromosome:: 7:76623192 (GRCh38)
7:76252509 (GRCh37)
Canonical SPDI:: NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:76623185:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
-=0.1649/826 (1000Genomes)
HGVS:: NC_000007.14:g.76623192_76623197del, NC_000007.14:g.76623193_76623197del, NC_000007.14:g.76623194_76623197del, NC_000007.14:g.76623195_76623197del, NC_000007.14:g.76623196_76623197del, NC_000007.14:g.76623197del, NC_000007.14:g.76623197dup, NC_000007.14:g.76623196_76623197dup, NC_000007.14:g.76623194_76623197dup, NC_000007.13:g.76252509_76252514del, NC_000007.13:g.76252510_76252514del, NC_000007.13:g.76252511_76252514del, NC_000007.13:g.76252512_76252514del, NC_000007.13:g.76252513_76252514del, NC_000007.13:g.76252514del, NC_000007.13:g.76252514dup, NC_000007.13:g.76252513_76252514dup, NC_000007.13:g.76252511_76252514dup, NT_187561.1:g.110027_110032del, NT_187561.1:g.110028_110032del, NT_187561.1:g.110029_110032del, NT_187561.1:g.110030_110032del, NT_187561.1:g.110031_110032del, NT_187561.1:g.110032del, NT_187561.1:g.110032dup, NT_187561.1:g.110031_110032dup, NT_187561.1:g.110029_110032dup

Select item 149097578215.

rs1490975782 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 7:76613503 (GRCh38)
7:76242820 (GRCh37)
Canonical SPDI:: NC_000007.14:76613502:T:A,NC_000007.14:76613502:T:C,NC_000007.14:76613502:T:G
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.00007/1 (TOMMO)
C=0.03453/94 (KOREAN)
HGVS:: NC_000007.14:g.76613503T>A, NC_000007.14:g.76613503T>C, NC_000007.14:g.76613503T>G, NC_000007.13:g.76242820T>A, NC_000007.13:g.76242820T>C, NC_000007.13:g.76242820T>G, NT_187561.1:g.100338T>A, NT_187561.1:g.100338T>C, NT_187561.1:g.100338T>G

Select item 149078192816.

rs1490781928 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:76621348 (GRCh38)
7:76250665 (GRCh37)
Canonical SPDI:: NC_000007.14:76621347:T:C
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000007.14:g.76621348T>C, NC_000007.13:g.76250665T>C, NT_187561.1:g.108183T>C

Select item 149074437817.

rs1490744378 has merged into rs768106589 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAAA [Show Flanks]
Chromosome:: 7:76620342 (GRCh38)
7:76249659 (GRCh37)
Canonical SPDI:: NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000007.14:76620329:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.45/18 (GENOME_DK)
HGVS:: NC_000007.14:g.76620342_76620347del, NC_000007.14:g.76620343_76620347del, NC_000007.14:g.76620344_76620347del, NC_000007.14:g.76620345_76620347del, NC_000007.14:g.76620346_76620347del, NC_000007.14:g.76620347del, NC_000007.14:g.76620347dup, NC_000007.14:g.76620346_76620347dup, NC_000007.14:g.76620343_76620347dup, NC_000007.13:g.76249659_76249664del, NC_000007.13:g.76249660_76249664del, NC_000007.13:g.76249661_76249664del, NC_000007.13:g.76249662_76249664del, NC_000007.13:g.76249663_76249664del, NC_000007.13:g.76249664del, NC_000007.13:g.76249664dup, NC_000007.13:g.76249663_76249664dup, NC_000007.13:g.76249660_76249664dup, NT_187561.1:g.107177_107182del, NT_187561.1:g.107178_107182del, NT_187561.1:g.107179_107182del, NT_187561.1:g.107180_107182del, NT_187561.1:g.107181_107182del, NT_187561.1:g.107182del, NT_187561.1:g.107182dup, NT_187561.1:g.107181_107182dup, NT_187561.1:g.107178_107182dup

Select item 149070871818.

rs1490708718 has merged into rs56084078 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 7:76620874 (GRCh38)
7:76250191 (GRCh37)
Canonical SPDI:: NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000007.14:76620861:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000007.14:g.76620874_76620886del, NC_000007.14:g.76620875_76620886del, NC_000007.14:g.76620876_76620886del, NC_000007.14:g.76620877_76620886del, NC_000007.14:g.76620878_76620886del, NC_000007.14:g.76620879_76620886del, NC_000007.14:g.76620880_76620886del, NC_000007.14:g.76620881_76620886del, NC_000007.14:g.76620882_76620886del, NC_000007.14:g.76620883_76620886del, NC_000007.14:g.76620884_76620886del, NC_000007.14:g.76620885_76620886del, NC_000007.14:g.76620886del, NC_000007.14:g.76620886dup, NC_000007.14:g.76620885_76620886dup, NC_000007.14:g.76620884_76620886dup, NC_000007.14:g.76620883_76620886dup, NC_000007.14:g.76620882_76620886dup, NC_000007.14:g.76620881_76620886dup, NC_000007.14:g.76620880_76620886dup, NC_000007.14:g.76620879_76620886dup, NC_000007.14:g.76620878_76620886dup, NC_000007.14:g.76620877_76620886dup, NC_000007.14:g.76620876_76620886dup, NC_000007.14:g.76620875_76620886dup, NC_000007.14:g.76620874_76620886dup, NC_000007.14:g.76620873_76620886dup, NC_000007.14:g.76620871_76620886dup, NC_000007.14:g.76620870_76620886dup, NC_000007.14:g.76620867_76620886dup, NC_000007.14:g.76620886_76620887insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000007.13:g.76250191_76250203del, NC_000007.13:g.76250192_76250203del, NC_000007.13:g.76250193_76250203del, NC_000007.13:g.76250194_76250203del, NC_000007.13:g.76250195_76250203del, NC_000007.13:g.76250196_76250203del, NC_000007.13:g.76250197_76250203del, NC_000007.13:g.76250198_76250203del, NC_000007.13:g.76250199_76250203del, NC_000007.13:g.76250200_76250203del, NC_000007.13:g.76250201_76250203del, NC_000007.13:g.76250202_76250203del, NC_000007.13:g.76250203del, NC_000007.13:g.76250203dup, NC_000007.13:g.76250202_76250203dup, NC_000007.13:g.76250201_76250203dup, NC_000007.13:g.76250200_76250203dup, NC_000007.13:g.76250199_76250203dup, NC_000007.13:g.76250198_76250203dup, NC_000007.13:g.76250197_76250203dup, NC_000007.13:g.76250196_76250203dup, NC_000007.13:g.76250195_76250203dup, NC_000007.13:g.76250194_76250203dup, NC_000007.13:g.76250193_76250203dup, NC_000007.13:g.76250192_76250203dup, NC_000007.13:g.76250191_76250203dup, NC_000007.13:g.76250190_76250203dup, NC_000007.13:g.76250188_76250203dup, NC_000007.13:g.76250187_76250203dup, NC_000007.13:g.76250184_76250203dup, NC_000007.13:g.76250203_76250204insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187561.1:g.107709_107721del, NT_187561.1:g.107710_107721del, NT_187561.1:g.107711_107721del, NT_187561.1:g.107712_107721del, NT_187561.1:g.107713_107721del, NT_187561.1:g.107714_107721del, NT_187561.1:g.107715_107721del, NT_187561.1:g.107716_107721del, NT_187561.1:g.107717_107721del, NT_187561.1:g.107718_107721del, NT_187561.1:g.107719_107721del, NT_187561.1:g.107720_107721del, NT_187561.1:g.107721del, NT_187561.1:g.107721dup, NT_187561.1:g.107720_107721dup, NT_187561.1:g.107719_107721dup, NT_187561.1:g.107718_107721dup, NT_187561.1:g.107717_107721dup, NT_187561.1:g.107716_107721dup, NT_187561.1:g.107715_107721dup, NT_187561.1:g.107714_107721dup, NT_187561.1:g.107713_107721dup, NT_187561.1:g.107712_107721dup, NT_187561.1:g.107711_107721dup, NT_187561.1:g.107710_107721dup, NT_187561.1:g.107709_107721dup, NT_187561.1:g.107708_107721dup, NT_187561.1:g.107706_107721dup, NT_187561.1:g.107705_107721dup, NT_187561.1:g.107702_107721dup, NT_187561.1:g.107721_107722insTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149058354919.

rs1490583549 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:76620052 (GRCh38)
7:76249369 (GRCh37)
Canonical SPDI:: NC_000007.14:76620051:T:C
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000007.14:g.76620052T>C, NC_000007.13:g.76249369T>C, NT_187561.1:g.106887T>C

Select item 149029721820.

rs1490297218 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:76621827 (GRCh38)
7:76251144 (GRCh37)
Canonical SPDI:: NC_000007.14:76621826:C:G
Gene:: POMZP3 (Varview), LINC03009 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.76621827C>G, NC_000007.13:g.76251144C>G, NT_187561.1:g.108662C>G

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