SNP Links for Gene (Select 55366) - SNP

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Select item 14915680141.

rs1491568014 has merged into rs10659783 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA [Show Flanks]
Chromosome:: 11:27456323 (GRCh38)
11:27477870 (GRCh37)
Canonical SPDI:: NC_000011.10:27456317:ACACACA:ACACA,NC_000011.10:27456317:ACACACA:ACACACACA
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACACA=0.258153/4781 (ALFA)
-=0.2/8 (GENOME_DK)
-=0.221429/992 (Estonian)
-=0.242485/242 (GoNL)
-=0.274964/38451 (GnomAD)
-=0.295145/78122 (TOPMED)
-=0.303873/1522 (1000Genomes)
-=0.313333/188 (NorthernSweden)
-=0.458631/7686 (TOMMO)
HGVS:: NC_000011.10:g.27456319CA[2], NC_000011.10:g.27456319CA[4], NC_000011.9:g.27477866CA[2], NC_000011.9:g.27477866CA[4], NG_051818.1:g.21453GT[2], NG_051818.1:g.21453GT[4]

Select item 14915461052.

rs1491546105 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 11:27391251 (GRCh38)
11:27412798 (GRCh37)
Canonical SPDI:: NC_000011.10:27391250:TC:
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00093/11 (ALFA)
HGVS:: NC_000011.10:g.27391251_27391252del, NC_000011.9:g.27412798_27412799del, NG_051818.1:g.86524_86525del

Select item 14915376863.

rs1491537686 [Homo sapiens]

Variant type:: DEL
Alleles:: GC>- [Show Flanks]
Chromosome:: 11:27385810 (GRCh38)
11:27407357 (GRCh37)
Canonical SPDI:: NC_000011.10:27385809:GC:
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.0002/1 (ALFA)
-=0.0002/1 (Estonian)
HGVS:: NC_000011.10:g.27385810_27385811del, NC_000011.9:g.27407357_27407358del, NG_051818.1:g.91965_91966del

Select item 14914824844.

rs1491482484 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTGT [Show Flanks]
Chromosome:: 11:27437661 (GRCh38)
11:27459209 (GRCh37)
Canonical SPDI:: NC_000011.10:27437661:TGT:TGTCTGT
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TGTCTGT=0./0 (ALFA)
HGVS:: NC_000011.10:g.27437664_27437665insCTGT, NC_000011.9:g.27459211_27459212insCTGT, NG_051818.1:g.40114_40115insGACA

Select item 14914573235.

rs1491457323 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 11:27449640 (GRCh38)
11:27471187 (GRCh37)
Canonical SPDI:: NC_000011.10:27449638:AGA:A
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.27449640_27449641del, NC_000011.9:g.27471187_27471188del, NG_051818.1:g.28136_28137del

Select item 14914403146.

rs1491440314 has merged into rs1336757147 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGGGG>-,G,GG,GGG,GGGG,GGGGGG,GGGGGGG,GGGGGGGG,GGGGGGGGG,GGGGGGGGGGGGGG [Show Flanks]
Chromosome:: 11:27393950 (GRCh38)
11:27415497 (GRCh37)
Canonical SPDI:: NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG,NC_000011.10:27393939:GGGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGGG
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGGGGG=0./0 (ALFA)
HGVS:: NC_000011.10:g.27393950_27393954del, NC_000011.10:g.27393951_27393954del, NC_000011.10:g.27393952_27393954del, NC_000011.10:g.27393953_27393954del, NC_000011.10:g.27393954del, NC_000011.10:g.27393954dup, NC_000011.10:g.27393953_27393954dup, NC_000011.10:g.27393952_27393954dup, NC_000011.10:g.27393951_27393954dup, NC_000011.10:g.27393946_27393954dup, NC_000011.9:g.27415497_27415501del, NC_000011.9:g.27415498_27415501del, NC_000011.9:g.27415499_27415501del, NC_000011.9:g.27415500_27415501del, NC_000011.9:g.27415501del, NC_000011.9:g.27415501dup, NC_000011.9:g.27415500_27415501dup, NC_000011.9:g.27415499_27415501dup, NC_000011.9:g.27415498_27415501dup, NC_000011.9:g.27415493_27415501dup, NG_051818.1:g.83832_83836del, NG_051818.1:g.83833_83836del, NG_051818.1:g.83834_83836del, NG_051818.1:g.83835_83836del, NG_051818.1:g.83836del, NG_051818.1:g.83836dup, NG_051818.1:g.83835_83836dup, NG_051818.1:g.83834_83836dup, NG_051818.1:g.83833_83836dup, NG_051818.1:g.83828_83836dup

Select item 14914398327.

rs1491439832 has merged into rs35556457 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT [Show Flanks]
Chromosome:: 11:27391248 (GRCh38)
11:27412795 (GRCh37)
Canonical SPDI:: NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000011.10:27391235:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
TT=0.0216/108 (1000Genomes)
HGVS:: NC_000011.10:g.27391248_27391251del, NC_000011.10:g.27391249_27391251del, NC_000011.10:g.27391250_27391251del, NC_000011.10:g.27391251del, NC_000011.10:g.27391251dup, NC_000011.10:g.27391250_27391251dup, NC_000011.10:g.27391249_27391251dup, NC_000011.10:g.27391248_27391251dup, NC_000011.10:g.27391247_27391251dup, NC_000011.10:g.27391246_27391251dup, NC_000011.10:g.27391245_27391251dup, NC_000011.9:g.27412795_27412798del, NC_000011.9:g.27412796_27412798del, NC_000011.9:g.27412797_27412798del, NC_000011.9:g.27412798del, NC_000011.9:g.27412798dup, NC_000011.9:g.27412797_27412798dup, NC_000011.9:g.27412796_27412798dup, NC_000011.9:g.27412795_27412798dup, NC_000011.9:g.27412794_27412798dup, NC_000011.9:g.27412793_27412798dup, NC_000011.9:g.27412792_27412798dup, NG_051818.1:g.86537_86540del, NG_051818.1:g.86538_86540del, NG_051818.1:g.86539_86540del, NG_051818.1:g.86540del, NG_051818.1:g.86540dup, NG_051818.1:g.86539_86540dup, NG_051818.1:g.86538_86540dup, NG_051818.1:g.86537_86540dup, NG_051818.1:g.86536_86540dup, NG_051818.1:g.86535_86540dup, NG_051818.1:g.86534_86540dup

Select item 14914271568.

rs1491427156 [Homo sapiens]

Variant type:: INS
Alleles:: ->C,T [Show Flanks]
Chromosome:: 11:27393940 (GRCh38)
11:27415488 (GRCh37)
Canonical SPDI:: NC_000011.10:27393940::C,NC_000011.10:27393940::T
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.27393940_27393941insC, NC_000011.10:g.27393940_27393941insT, NC_000011.9:g.27415487_27415488insC, NC_000011.9:g.27415487_27415488insT, NG_051818.1:g.83835_83836insG, NG_051818.1:g.83835_83836insA

Select item 14914058079.

rs1491405807 [Homo sapiens]

Variant type:: INS
Alleles:: ->TTC,TTTC,TTTTC,TTTTTA [Show Flanks]
Chromosome:: 11:27391251 (GRCh38)
11:27412799 (GRCh37)
Canonical SPDI:: NC_000011.10:27391251::TTC,NC_000011.10:27391251::TTTC,NC_000011.10:27391251::TTTTC,NC_000011.10:27391251::TTTTTA
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTC=0./0 (ALFA)
HGVS:: NC_000011.10:g.27391251_27391252insTTC, NC_000011.10:g.27391251_27391252insTTTC, NC_000011.10:g.27391251_27391252insTTTTC, NC_000011.10:g.27391251_27391252insTTTTTA, NC_000011.9:g.27412798_27412799insTTC, NC_000011.9:g.27412798_27412799insTTTC, NC_000011.9:g.27412798_27412799insTTTTC, NC_000011.9:g.27412798_27412799insTTTTTA, NG_051818.1:g.86524_86525insGAA, NG_051818.1:g.86524_86525insGAAA, NG_051818.1:g.86524_86525insGAAAA, NG_051818.1:g.86524_86525insTAAAAA

Select item 149137056310.

rs1491370563 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 11:27452645 (GRCh38)
11:27474192 (GRCh37)
Canonical SPDI:: NC_000011.10:27452644:TG:
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00024/28 (GnomAD)
HGVS:: NC_000011.10:g.27452645_27452646del, NC_000011.9:g.27474192_27474193del, NG_051818.1:g.25130_25131del

Select item 149129254711.

rs1491292547 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 11:27461632 (GRCh38)
11:27483179 (GRCh37)
Canonical SPDI:: NC_000011.10:27461631:AT:
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000016/2 (GnomAD)
HGVS:: NC_000011.10:g.27461632_27461633del, NC_000011.9:g.27483179_27483180del, NG_051818.1:g.16143_16144del

Select item 149129247412.

rs1491292474 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAAG [Show Flanks]
Chromosome:: 11:27436350 (GRCh38)
11:27457898 (GRCh37)
Canonical SPDI:: NC_000011.10:27436350:AAG:AAGTAAG
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AAGTAAG=0./0 (ALFA)
AAGT=0.000009/1 (GnomAD)
HGVS:: NC_000011.10:g.27436353_27436354insTAAG, NC_000011.9:g.27457900_27457901insTAAG, NG_051818.1:g.41425_41426insACTT

Select item 149123556213.

rs1491235562 has merged into rs59633176 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 11:27454772 (GRCh38)
11:27476319 (GRCh37)
Canonical SPDI:: NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000011.10:27454761:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.1893/103 (NorthernSweden)
A=0.475/19 (GENOME_DK)
HGVS:: NC_000011.10:g.27454772_27454777del, NC_000011.10:g.27454773_27454777del, NC_000011.10:g.27454774_27454777del, NC_000011.10:g.27454775_27454777del, NC_000011.10:g.27454776_27454777del, NC_000011.10:g.27454777del, NC_000011.10:g.27454777dup, NC_000011.10:g.27454776_27454777dup, NC_000011.10:g.27454775_27454777dup, NC_000011.10:g.27454771_27454777dup, NC_000011.10:g.27454765_27454777dup, NC_000011.9:g.27476319_27476324del, NC_000011.9:g.27476320_27476324del, NC_000011.9:g.27476321_27476324del, NC_000011.9:g.27476322_27476324del, NC_000011.9:g.27476323_27476324del, NC_000011.9:g.27476324del, NC_000011.9:g.27476324dup, NC_000011.9:g.27476323_27476324dup, NC_000011.9:g.27476322_27476324dup, NC_000011.9:g.27476318_27476324dup, NC_000011.9:g.27476312_27476324dup, NG_051818.1:g.23009_23014del, NG_051818.1:g.23010_23014del, NG_051818.1:g.23011_23014del, NG_051818.1:g.23012_23014del, NG_051818.1:g.23013_23014del, NG_051818.1:g.23014del, NG_051818.1:g.23014dup, NG_051818.1:g.23013_23014dup, NG_051818.1:g.23012_23014dup, NG_051818.1:g.23008_23014dup, NG_051818.1:g.23002_23014dup

Select item 149123059414.

rs1491230594 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CGG [Show Flanks]
Chromosome:: 11:27393939 (GRCh38)
11:27415487 (GRCh37)
Canonical SPDI:: NC_000011.10:27393939:GG:GGCGG
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GGCGG=0./0 (ALFA)
GGC=0.0001/1 (GnomAD)
HGVS:: NC_000011.10:g.27393941_27393942insCGG, NC_000011.9:g.27415488_27415489insCGG, NG_051818.1:g.83836_83837insGCC

Select item 149118946915.

rs1491189469 [Homo sapiens]

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

Select item 149114809316.

rs1491148093 [Homo sapiens]

Variant type:: INS
Alleles:: ->AA [Show Flanks]
Chromosome:: 11:27385810 (GRCh38)
11:27407358 (GRCh37)
Canonical SPDI:: NC_000011.10:27385810::AA
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: AA=0.0007/3 (Estonian)
HGVS:: NC_000011.10:g.27385810_27385811insAA, NC_000011.9:g.27407357_27407358insAA, NG_051818.1:g.91965_91966insTT

Select item 149114695517.

rs1491146955 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 11:27393939 (GRCh38)
11:27415486 (GRCh37)
Canonical SPDI:: NC_000011.10:27393938:TG:
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00368/42 (ALFA)
-=0.00004/1 (TOMMO)
-=0.22484/898 (GnomAD)
HGVS:: NC_000011.10:g.27393939_27393940del, NC_000011.9:g.27415486_27415487del, NG_051818.1:g.83836_83837del

Select item 149111226018.

rs1491112260 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 11:27391235 (GRCh38)
11:27412782 (GRCh37)
Canonical SPDI:: NC_000011.10:27391234:CT:
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00008/1 (ALFA)
-=0.00016/3 (GnomAD)
HGVS:: NC_000011.10:g.27391235_27391236del, NC_000011.9:g.27412782_27412783del, NG_051818.1:g.86540_86541del

Select item 149103895619.

rs1491038956 has merged into rs3085345 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA [Show Flanks]
Chromosome:: 11:27381716 (GRCh38)
11:27403263 (GRCh37)
Canonical SPDI:: NC_000011.10:27381706:AAAAAAAAAAA:AAAAAAAAA,NC_000011.10:27381706:AAAAAAAAAAA:AAAAAAAAAA,NC_000011.10:27381706:AAAAAAAAAAA:AAAAAAAAAAAA,NC_000011.10:27381706:AAAAAAAAAAA:AAAAAAAAAAAAA
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0.0004/2 (ALFA)
A=0.0769/385 (1000Genomes)
HGVS:: NC_000011.10:g.27381716_27381717del, NC_000011.10:g.27381717del, NC_000011.10:g.27381717dup, NC_000011.10:g.27381716_27381717dup, NC_000011.9:g.27403263_27403264del, NC_000011.9:g.27403264del, NC_000011.9:g.27403264dup, NC_000011.9:g.27403263_27403264dup, NG_051818.1:g.96068_96069del, NG_051818.1:g.96069del, NG_051818.1:g.96069dup, NG_051818.1:g.96068_96069dup

Select item 149103085720.

rs1491030857 has merged into rs55877673 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 11:27418841 (GRCh38)
11:27440388 (GRCh37)
Canonical SPDI:: NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000011.10:27418832:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
Gene:: LGR4 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.33606/1683 (1000Genomes)
HGVS:: NC_000011.10:g.27418841_27418850del, NC_000011.10:g.27418844_27418850del, NC_000011.10:g.27418846_27418850del, NC_000011.10:g.27418847_27418850del, NC_000011.10:g.27418848_27418850del, NC_000011.10:g.27418849_27418850del, NC_000011.10:g.27418850del, NC_000011.10:g.27418850dup, NC_000011.10:g.27418849_27418850dup, NC_000011.10:g.27418848_27418850dup, NC_000011.10:g.27418847_27418850dup, NC_000011.9:g.27440388_27440397del, NC_000011.9:g.27440391_27440397del, NC_000011.9:g.27440393_27440397del, NC_000011.9:g.27440394_27440397del, NC_000011.9:g.27440395_27440397del, NC_000011.9:g.27440396_27440397del, NC_000011.9:g.27440397del, NC_000011.9:g.27440397dup, NC_000011.9:g.27440396_27440397dup, NC_000011.9:g.27440395_27440397dup, NC_000011.9:g.27440394_27440397dup, NG_051818.1:g.58934_58943del, NG_051818.1:g.58937_58943del, NG_051818.1:g.58939_58943del, NG_051818.1:g.58940_58943del, NG_051818.1:g.58941_58943del, NG_051818.1:g.58942_58943del, NG_051818.1:g.58943del, NG_051818.1:g.58943dup, NG_051818.1:g.58942_58943dup, NG_051818.1:g.58941_58943dup, NG_051818.1:g.58940_58943dup

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