rs869025217

Orientation

plus

Stabilized

plus

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

Make rs869025217(A;A)

Make rs869025217(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

184170318

Gene

DVL3

is a	snp
is	mentioned by
dbSNP	rs869025217
dbSNP (classic)	rs869025217
ClinGen	rs869025217
ebi	rs869025217
HLI	rs869025217
Exac	rs869025217
Gnomad	rs869025217
Varsome	rs869025217
LitVar	rs869025217
Map	rs869025217
PheGenI	rs869025217
Biobank	rs869025217
1000 genomes	rs869025217
hgdp	rs869025217
ensembl	rs869025217
geneview	rs869025217
scholar	rs869025217
google	rs869025217
pharmgkb	rs869025217
gwascentral	rs869025217
openSNP	rs869025217
23andMe	rs869025217
SNPshot	rs869025217
SNPdbe	rs869025217
MSV3d	rs869025217
GWAS Ctlg	rs869025217

Max Magnitude

0

ClinVar
Risk	rs869025217(A;A)
Alt	rs869025217(A;A)
Reference	Rs869025217(G;G)
Significance	Pathogenic
Disease	Robinow syndrome Robinow syndrome
Variation	info
Gene	DVL3
CLNDBN	Robinow syndrome Robinow syndrome, autosomal dominant 3
Reversed	0
HGVS	NC_000003.11:g.183888106G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000208714.1, RCV000210483.1,