rs786204837

Orientation

minus

Stabilized

minus

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

Make rs786204837(A;A)

Make rs786204837(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

55479499

Gene

WNT5A

is a	snp
is	mentioned by
dbSNP	rs786204837
dbSNP (classic)	rs786204837
ClinGen	rs786204837
ebi	rs786204837
HLI	rs786204837
Exac	rs786204837
Gnomad	rs786204837
Varsome	rs786204837
LitVar	rs786204837
Map	rs786204837
PheGenI	rs786204837
Biobank	rs786204837
1000 genomes	rs786204837
hgdp	rs786204837
ensembl	rs786204837
geneview	rs786204837
scholar	rs786204837
google	rs786204837
pharmgkb	rs786204837
gwascentral	rs786204837
openSNP	rs786204837
23andMe	rs786204837
SNPshot	rs786204837
SNPdbe	rs786204837
MSV3d	rs786204837
GWAS Ctlg	rs786204837

Max Magnitude

0

ClinVar
Risk	rs786204837(A;A)
Alt	rs786204837(A;A)
Reference	Rs786204837(G;G)
Significance	Pathogenic
Disease	Robinow syndrome
Variation	info
Gene	WNT5A
CLNDBN	Robinow syndrome
Reversed	1
HGVS	NC_000003.11:g.55513527C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000169741.5,