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rs767569346

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767569346(A;A)
Make rs767569346(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position14158206
GeneXPC
is asnp
is mentioned by
dbSNPrs767569346
ebirs767569346
HLIrs767569346
Exacrs767569346
Varsomers767569346
Maprs767569346
PheGenIrs767569346
hapmaprs767569346
1000 genomesrs767569346
hgdprs767569346
ensemblrs767569346
gopubmedrs767569346
geneviewrs767569346
scholarrs767569346
googlers767569346
pharmgkbrs767569346
gwascentralrs767569346
openSNPrs767569346
23andMers767569346
23andMe allrs767569346
SNP Nexus

SNPshotrs767569346
SNPdbers767569346
MSV3drs767569346
GWAS Ctlgrs767569346
Max Magnitude0
ClinVar
Risk rs767569346(A,C,T;A,C,T)
Alt rs767569346(A,C,T;A,C,T)
Reference rs767569346(G;G)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene XPC
CLNDBN Xeroderma pigmentosum, group C
Reversed 0
HGVS NC_000003.11:g.14199706G>T
CLNSRC
CLNACC RCV000170432.1,