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rs267607281

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607281(A;A)
Make rs267607281(A;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position102846349
GeneBIVM-ERCC5, ERCC5
is asnp
is mentioned by
dbSNPrs267607281
ebirs267607281
HLIrs267607281
Exacrs267607281
Varsomers267607281
Maprs267607281
PheGenIrs267607281
hapmaprs267607281
1000 genomesrs267607281
hgdprs267607281
ensemblrs267607281
gopubmedrs267607281
geneviewrs267607281
scholarrs267607281
googlers267607281
pharmgkbrs267607281
gwascentralrs267607281
openSNPrs267607281
23andMers267607281
23andMe allrs267607281
SNP Nexus

SNPshotrs267607281
SNPdbers267607281
MSV3drs267607281
GWAS Ctlgrs267607281
Max Magnitude0
ClinVar
Risk rs267607281(A;A)
Alt rs267607281(A;A)
Reference rs267607281(C;C)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene BIVM-ERCC5 ERCC5
CLNDBN Xeroderma pigmentosum, group G
Reversed 0
HGVS NC_000013.10:g.103498699C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000034376.26,