rs121908652

Orientation

minus

Stabilized

minus

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

Make rs121908652(C;T)

Make rs121908652(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

22129682

Gene

WNT4

is a	snp
is	mentioned by
dbSNP	rs121908652
dbSNP (classic)	rs121908652
ClinGen	rs121908652
ebi	rs121908652
HLI	rs121908652
Exac	rs121908652
Gnomad	rs121908652
Varsome	rs121908652
LitVar	rs121908652
Map	rs121908652
PheGenI	rs121908652
Biobank	rs121908652
1000 genomes	rs121908652
hgdp	rs121908652
ensembl	rs121908652
geneview	rs121908652
scholar	rs121908652
google	rs121908652
pharmgkb	rs121908652
gwascentral	rs121908652
openSNP	rs121908652
23andMe	rs121908652
SNPshot	rs121908652
SNPdbe	rs121908652
MSV3d	rs121908652
GWAS Ctlg	rs121908652

Max Magnitude

0

OMIM	603490
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121908652(T;T)
Alt	rs121908652(T;T)
Reference	Rs121908652(C;C)
Significance	Pathogenic
Disease	Mullerian aplasia and hyperandrogenism
Variation	info
Gene	WNT4
CLNDBN	Mullerian aplasia and hyperandrogenism
Reversed	1
HGVS	NC_000001.10:g.22456175G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000006690.2,