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rs267606692

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606692(C;C)
Make rs267606692(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position63437430
GeneWDPCP
is asnp
is mentioned by
dbSNPrs267606692
ebirs267606692
HLIrs267606692
Exacrs267606692
Varsomers267606692
Maprs267606692
PheGenIrs267606692
hapmaprs267606692
1000 genomesrs267606692
hgdprs267606692
ensemblrs267606692
gopubmedrs267606692
geneviewrs267606692
scholarrs267606692
googlers267606692
pharmgkbrs267606692
gwascentralrs267606692
openSNPrs267606692
23andMers267606692
23andMe allrs267606692
SNP Nexus

SNPshotrs267606692
SNPdbers267606692
MSV3drs267606692
GWAS Ctlgrs267606692
Max Magnitude0
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,