rs786204836

Orientation

minus

Stabilized

minus

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

Make rs786204836(A;G)

Make rs786204836(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

3

Position

55479448

Gene

WNT5A

is a	snp
is	mentioned by
dbSNP	rs786204836
dbSNP (classic)	rs786204836
ClinGen	rs786204836
ebi	rs786204836
HLI	rs786204836
Exac	rs786204836
Gnomad	rs786204836
Varsome	rs786204836
LitVar	rs786204836
Map	rs786204836
PheGenI	rs786204836
Biobank	rs786204836
1000 genomes	rs786204836
hgdp	rs786204836
ensembl	rs786204836
geneview	rs786204836
scholar	rs786204836
google	rs786204836
pharmgkb	rs786204836
gwascentral	rs786204836
openSNP	rs786204836
23andMe	rs786204836
SNPshot	rs786204836
SNPdbe	rs786204836
MSV3d	rs786204836
GWAS Ctlg	rs786204836

Max Magnitude

0

ClinVar
Risk	rs786204836(G;G)
Alt	rs786204836(G;G)
Reference	Rs786204836(A;A)
Significance	Pathogenic
Disease	Robinow syndrome
Variation	info
Gene	WNT5A
CLNDBN	Robinow syndrome
Reversed	1
HGVS	NC_000003.11:g.55513476T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000169740.5,