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rs759607901

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759607901(C;T)
Make rs759607901(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position43604637
GenePOLH
is asnp
is mentioned by
dbSNPrs759607901
ebirs759607901
HLIrs759607901
Exacrs759607901
Varsomers759607901
Maprs759607901
PheGenIrs759607901
hapmaprs759607901
1000 genomesrs759607901
hgdprs759607901
ensemblrs759607901
gopubmedrs759607901
geneviewrs759607901
scholarrs759607901
googlers759607901
pharmgkbrs759607901
gwascentralrs759607901
openSNPrs759607901
23andMers759607901
23andMe allrs759607901
SNP Nexus

SNPshotrs759607901
SNPdbers759607901
MSV3drs759607901
GWAS Ctlgrs759607901
Max Magnitude0
ClinVar
Risk rs759607901(T;T)
Alt rs759607901(T;T)
Reference rs759607901(C;C)
Significance Pathogenic
Disease Xeroderma pigmentosum
Variation info
Gene POLH
CLNDBN Xeroderma pigmentosum, variant type
Reversed 0
HGVS NC_000006.11:g.43572374C>T
CLNSRC
CLNACC RCV000209179.1,