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rs794729655

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729655(G;G)
Make rs794729655(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position14156333
GeneXPC
is asnp
is mentioned by
dbSNPrs794729655
ebirs794729655
HLIrs794729655
Exacrs794729655
Varsomers794729655
Maprs794729655
PheGenIrs794729655
hapmaprs794729655
1000 genomesrs794729655
hgdprs794729655
ensemblrs794729655
gopubmedrs794729655
geneviewrs794729655
scholarrs794729655
googlers794729655
pharmgkbrs794729655
gwascentralrs794729655
openSNPrs794729655
23andMers794729655
23andMe allrs794729655
SNP Nexus

SNPshotrs794729655
SNPdbers794729655
MSV3drs794729655
GWAS Ctlgrs794729655
Max Magnitude0
ClinVar
Risk rs794729655(G;G)
Alt rs794729655(G;G)
Reference rs794729655(T;T)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene XPC
CLNDBN Xeroderma pigmentosum, group C
Reversed 1
HGVS NC_000003.11:g.14197833A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000281.2,