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rs41270025

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs41270025(G;T)
Make rs41270025(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161168463
GenePPOX
is asnp
is mentioned by
dbSNPrs41270025
ebirs41270025
HLIrs41270025
Exacrs41270025
Varsomers41270025
Maprs41270025
PheGenIrs41270025
hapmaprs41270025
1000 genomesrs41270025
hgdprs41270025
ensemblrs41270025
gopubmedrs41270025
geneviewrs41270025
scholarrs41270025
googlers41270025
pharmgkbrs41270025
gwascentralrs41270025
openSNPrs41270025
23andMers41270025
23andMe allrs41270025
SNP Nexus

SNPshotrs41270025
SNPdbers41270025
MSV3drs41270025
GWAS Ctlgrs41270025
Max Magnitude0
OMIM600923
Desc
Variant0006
Relatedalso


ClinVar
Risk rs41270025(A,T;A,T)
Alt rs41270025(A,T;A,T)
Reference rs41270025(G;G)
Significance Pathogenic
Disease Variegate porphyria
Variation info
Gene PPOX
CLNDBN Variegate porphyria
Reversed 0
HGVS NC_000001.10:g.161138253G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009234.4,