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rs267606693

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606693(A;A)
Make rs267606693(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position63487491
GeneWDPCP
is asnp
is mentioned by
dbSNPrs267606693
ebirs267606693
HLIrs267606693
Exacrs267606693
Varsomers267606693
Maprs267606693
PheGenIrs267606693
hapmaprs267606693
1000 genomesrs267606693
hgdprs267606693
ensemblrs267606693
gopubmedrs267606693
geneviewrs267606693
scholarrs267606693
googlers267606693
pharmgkbrs267606693
gwascentralrs267606693
openSNPrs267606693
23andMers267606693
23andMe allrs267606693
SNP Nexus

SNPshotrs267606693
SNPdbers267606693
MSV3drs267606693
GWAS Ctlgrs267606693
Max Magnitude0
ClinVar
Risk rs267606693(A;A)
Alt rs267606693(A;A)
Reference rs267606693(G;G)
Significance Other
Disease Meckel syndrome
Variation info
Gene WDPCP
CLNDBN Meckel syndrome, type 6, modifier of
Reversed 1
HGVS NC_000002.11:g.63714625C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000064.5,