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rs794729656

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs794729656(A;A)
Make rs794729656(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position14168389
GeneXPC
is asnp
is mentioned by
dbSNPrs794729656
ebirs794729656
HLIrs794729656
Exacrs794729656
Varsomers794729656
Maprs794729656
PheGenIrs794729656
hapmaprs794729656
1000 genomesrs794729656
hgdprs794729656
ensemblrs794729656
gopubmedrs794729656
geneviewrs794729656
scholarrs794729656
googlers794729656
pharmgkbrs794729656
gwascentralrs794729656
openSNPrs794729656
23andMers794729656
23andMe allrs794729656
SNP Nexus

SNPshotrs794729656
SNPdbers794729656
MSV3drs794729656
GWAS Ctlgrs794729656
Max Magnitude0
ClinVar
Risk rs794729656(A;A)
Alt rs794729656(A;A)
Reference rs794729656(T;T)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene XPC
CLNDBN Xeroderma pigmentosum, group C
Reversed 1
HGVS NC_000003.11:g.14209889A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000284.2,