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rs121908562

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908562(G;T)
Make rs121908562(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position43604646
GenePOLH
is asnp
is mentioned by
dbSNPrs121908562
ebirs121908562
HLIrs121908562
Exacrs121908562
Varsomers121908562
Maprs121908562
PheGenIrs121908562
hapmaprs121908562
1000 genomesrs121908562
hgdprs121908562
ensemblrs121908562
gopubmedrs121908562
geneviewrs121908562
scholarrs121908562
googlers121908562
pharmgkbrs121908562
gwascentralrs121908562
openSNPrs121908562
23andMers121908562
23andMe allrs121908562
SNP Nexus

SNPshotrs121908562
SNPdbers121908562
MSV3drs121908562
GWAS Ctlgrs121908562
Max Magnitude0
OMIM603968
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121908562(T;T)
Alt rs121908562(T;T)
Reference rs121908562(G;G)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene POLH
CLNDBN Xeroderma pigmentosum, variant type
Reversed 0
HGVS NC_000006.11:g.43572383G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000006245.2,