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rs74737358

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74737358(A;A)
Make rs74737358(A;C)
Make rs74737358(C;C)
ReferenceGRCh38 38.1/141
Chromosome3
Position14158882
GeneXPC
is asnp
is mentioned by
dbSNPrs74737358
ebirs74737358
HLIrs74737358
Exacrs74737358
Varsomers74737358
Maprs74737358
PheGenIrs74737358
hapmaprs74737358
1000 genomesrs74737358
hgdprs74737358
ensemblrs74737358
gopubmedrs74737358
geneviewrs74737358
scholarrs74737358
googlers74737358
pharmgkbrs74737358
gwascentralrs74737358
openSNPrs74737358
23andMers74737358
23andMe allrs74737358
SNP Nexus

SNPshotrs74737358
SNPdbers74737358
MSV3drs74737358
GWAS Ctlgrs74737358
GMAF0.003673
Max Magnitude0
OMIM613208
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74737358(A,C,T;A,C,T)
Alt rs74737358(A,C,T;A,C,T)
Reference rs74737358(G;G)
Significance Pathogenic
Disease Xeroderma pigmentosum not specified
Variation info
Gene XPC
CLNDBN Xeroderma pigmentosum, group C not specified
Reversed 0
HGVS NC_000003.11:g.14200382G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000277.2, RCV000122346.1,