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rs121908564

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908564(C;T)
Make rs121908564(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43610596
GenePOLH
is asnp
is mentioned by
dbSNPrs121908564
ebirs121908564
HLIrs121908564
Exacrs121908564
Varsomers121908564
Maprs121908564
PheGenIrs121908564
hapmaprs121908564
1000 genomesrs121908564
hgdprs121908564
ensemblrs121908564
gopubmedrs121908564
geneviewrs121908564
scholarrs121908564
googlers121908564
pharmgkbrs121908564
gwascentralrs121908564
openSNPrs121908564
23andMers121908564
23andMe allrs121908564
SNP Nexus

SNPshotrs121908564
SNPdbers121908564
MSV3drs121908564
GWAS Ctlgrs121908564
Max Magnitude0
OMIM603968
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121908564(T;T)
Alt rs121908564(T;T)
Reference rs121908564(C;C)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene POLH
CLNDBN Xeroderma pigmentosum, variant type
Reversed 0
HGVS NC_000006.11:g.43578333C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006248.2,