Have questions? Visit https://www.reddit.com/r/SNPedia

rs869025275

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025275(A;A)
Make rs869025275(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position14152417
GeneXPC
is asnp
is mentioned by
dbSNPrs869025275
ebirs869025275
HLIrs869025275
Exacrs869025275
Varsomers869025275
Maprs869025275
PheGenIrs869025275
hapmaprs869025275
1000 genomesrs869025275
hgdprs869025275
ensemblrs869025275
gopubmedrs869025275
geneviewrs869025275
scholarrs869025275
googlers869025275
pharmgkbrs869025275
gwascentralrs869025275
openSNPrs869025275
23andMers869025275
23andMe allrs869025275
SNP Nexus

SNPshotrs869025275
SNPdbers869025275
MSV3drs869025275
GWAS Ctlgrs869025275
Max Magnitude0
ClinVar
Risk rs869025275(A;A)
Alt rs869025275(A;A)
Reference rs869025275(G;G)
Significance Probable-Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene XPC
CLNDBN Xeroderma pigmentosum, type 1
Reversed 1
HGVS NC_000003.11:g.14193917C>T
CLNSRC
CLNACC RCV000207299.1,