rs121908651

Orientation

minus

Stabilized

minus

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

Make rs121908651(C;T)

Make rs121908651(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

22121549

Gene

WNT4

is a	snp
is	mentioned by
dbSNP	rs121908651
dbSNP (classic)	rs121908651
ClinGen	rs121908651
ebi	rs121908651
HLI	rs121908651
Exac	rs121908651
Gnomad	rs121908651
Varsome	rs121908651
LitVar	rs121908651
Map	rs121908651
PheGenI	rs121908651
Biobank	rs121908651
1000 genomes	rs121908651
hgdp	rs121908651
ensembl	rs121908651
geneview	rs121908651
scholar	rs121908651
google	rs121908651
pharmgkb	rs121908651
gwascentral	rs121908651
openSNP	rs121908651
23andMe	rs121908651
SNPshot	rs121908651
SNPdbe	rs121908651
MSV3d	rs121908651
GWAS Ctlg	rs121908651

Max Magnitude

0

OMIM	603490
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121908651(T;T)
Alt	rs121908651(T;T)
Reference	Rs121908651(C;C)
Significance	Pathogenic
Disease	Serkal syndrome
Variation	info
Gene	WNT4
CLNDBN	Serkal syndrome
Reversed	1
HGVS	NC_000001.10:g.22448042G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000006689.3,