rs267606692

Orientation

minus

Stabilized

minus

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

Make rs267606692(C;C)

Make rs267606692(C;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

63437430

Gene

WDPCP

is a	snp
is	mentioned by
dbSNP	rs267606692
dbSNP (classic)	rs267606692
ClinGen	rs267606692
ebi	rs267606692
HLI	rs267606692
Exac	rs267606692
Gnomad	rs267606692
Varsome	rs267606692
LitVar	rs267606692
Map	rs267606692
PheGenI	rs267606692
Biobank	rs267606692
1000 genomes	rs267606692
hgdp	rs267606692
ensembl	rs267606692
geneview	rs267606692
scholar	rs267606692
google	rs267606692
pharmgkb	rs267606692
gwascentral	rs267606692
openSNP	rs267606692
23andMe	rs267606692
SNPshot	rs267606692
SNPdbe	rs267606692
MSV3d	rs267606692
GWAS Ctlg	rs267606692

Max Magnitude

0

ClinVar
Risk	rs267606692(C;C)
Alt	rs267606692(C;C)
Reference	Rs267606692(G;G)
Significance	Other
Disease	Bardet-Biedl syndrome 12
Variation	info
Gene	WDPCP
CLNDBN	Bardet-Biedl syndrome 12, modifier of
Reversed	1
HGVS	NC_000002.11:g.63664564C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000000063.6,