rs869025215

Orientation

plus

Stabilized

plus

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

Make rs869025215(-;-)

Make rs869025215(-;G)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

184170092

Gene

DVL3

is a	snp
is	mentioned by
dbSNP	rs869025215
dbSNP (classic)	rs869025215
ClinGen	rs869025215
ebi	rs869025215
HLI	rs869025215
Exac	rs869025215
Gnomad	rs869025215
Varsome	rs869025215
LitVar	rs869025215
Map	rs869025215
PheGenI	rs869025215
Biobank	rs869025215
1000 genomes	rs869025215
hgdp	rs869025215
ensembl	rs869025215
geneview	rs869025215
scholar	rs869025215
google	rs869025215
pharmgkb	rs869025215
gwascentral	rs869025215
openSNP	rs869025215
23andMe	rs869025215
SNPshot	rs869025215
SNPdbe	rs869025215
MSV3d	rs869025215
GWAS Ctlg	rs869025215

Max Magnitude

0

ClinVar
Risk	rs869025215(-;-)
Alt	rs869025215(-;-)
Reference	Rs869025215(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.183887880delG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000208632.1, RCV000210480.1,