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rs201940931

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201940931(G;G)
Make rs201940931(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position14165587
GeneXPC
is asnp
is mentioned by
dbSNPrs201940931
ebirs201940931
HLIrs201940931
Exacrs201940931
Varsomers201940931
Maprs201940931
PheGenIrs201940931
hapmaprs201940931
1000 genomesrs201940931
hgdprs201940931
ensemblrs201940931
gopubmedrs201940931
geneviewrs201940931
scholarrs201940931
googlers201940931
pharmgkbrs201940931
gwascentralrs201940931
openSNPrs201940931
23andMers201940931
23andMe allrs201940931
SNP Nexus

SNPshotrs201940931
SNPdbers201940931
MSV3drs201940931
GWAS Ctlgrs201940931
Max Magnitude0
ClinVar
Risk rs201940931(G;G)
Alt rs201940931(G;G)
Reference rs201940931(T;T)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene XPC
CLNDBN Xeroderma pigmentosum, group C
Reversed 0
HGVS NC_000003.11:g.14207087T>G
CLNSRC
CLNACC RCV000170430.1,