rs869025218

Orientation

plus

Stabilized

plus

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

Make rs869025218(-;-)

Make rs869025218(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

3

Position

184170320

Gene

DVL3

is a	snp
is	mentioned by
dbSNP	rs869025218
dbSNP (classic)	rs869025218
ClinGen	rs869025218
ebi	rs869025218
HLI	rs869025218
Exac	rs869025218
Gnomad	rs869025218
Varsome	rs869025218
LitVar	rs869025218
Map	rs869025218
PheGenI	rs869025218
Biobank	rs869025218
1000 genomes	rs869025218
hgdp	rs869025218
ensembl	rs869025218
geneview	rs869025218
scholar	rs869025218
google	rs869025218
pharmgkb	rs869025218
gwascentral	rs869025218
openSNP	rs869025218
23andMe	rs869025218
SNPshot	rs869025218
SNPdbe	rs869025218
MSV3d	rs869025218
GWAS Ctlg	rs869025218

Max Magnitude

0

ClinVar
Risk	rs869025218(-;-)
Alt	rs869025218(-;-)
Reference	Rs869025218(C;C)
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.183888108delC
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000208637.1, RCV000210486.1,