rs121908650

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs121908650(A;G)

Make rs121908650(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

22120459

Gene

WNT4

is a	snp
is	mentioned by
dbSNP	rs121908650
dbSNP (classic)	rs121908650
ClinGen	rs121908650
ebi	rs121908650
HLI	rs121908650
Exac	rs121908650
Gnomad	rs121908650
Varsome	rs121908650
LitVar	rs121908650
Map	rs121908650
PheGenI	rs121908650
Biobank	rs121908650
1000 genomes	rs121908650
hgdp	rs121908650
ensembl	rs121908650
geneview	rs121908650
scholar	rs121908650
google	rs121908650
pharmgkb	rs121908650
gwascentral	rs121908650
openSNP	rs121908650
23andMe	rs121908650
SNPshot	rs121908650
SNPdbe	rs121908650
MSV3d	rs121908650
GWAS Ctlg	rs121908650

Max Magnitude

0

OMIM	603490
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908650(G;G)
Alt	rs121908650(G;G)
Reference	Rs121908650(A;A)
Significance	Pathogenic
Disease	Mullerian aplasia and hyperandrogenism
Variation	info
Gene	WNT4
CLNDBN	Mullerian aplasia and hyperandrogenism
Reversed	1
HGVS	NC_000001.10:g.22446952T>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006688.2,