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

rs754673606

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs754673606(C;T)
Make rs754673606(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position14148732
GeneXPC
is asnp
is mentioned by
dbSNPrs754673606
ebirs754673606
HLIrs754673606
Exacrs754673606
Varsomers754673606
Maprs754673606
PheGenIrs754673606
hapmaprs754673606
1000 genomesrs754673606
hgdprs754673606
ensemblrs754673606
gopubmedrs754673606
geneviewrs754673606
scholarrs754673606
googlers754673606
pharmgkbrs754673606
gwascentralrs754673606
openSNPrs754673606
23andMers754673606
23andMe allrs754673606
SNP Nexus

SNPshotrs754673606
SNPdbers754673606
MSV3drs754673606
GWAS Ctlgrs754673606
Max Magnitude0
ClinVar
Risk rs754673606(G,T;G,T)
Alt rs754673606(G,T;G,T)
Reference rs754673606(C;C)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene XPC
CLNDBN Xeroderma pigmentosum, group C
Reversed 0
HGVS NC_000003.11:g.14190232C>G
CLNSRC
CLNACC RCV000170434.1,