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rs121918324

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121918324(C;T)
Make rs121918324(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position161167187
GenePPOX
is asnp
is mentioned by
dbSNPrs121918324
ebirs121918324
HLIrs121918324
Exacrs121918324
Varsomers121918324
Maprs121918324
PheGenIrs121918324
hapmaprs121918324
1000 genomesrs121918324
hgdprs121918324
ensemblrs121918324
gopubmedrs121918324
geneviewrs121918324
scholarrs121918324
googlers121918324
pharmgkbrs121918324
gwascentralrs121918324
openSNPrs121918324
23andMers121918324
23andMe allrs121918324
SNP Nexus

SNPshotrs121918324
SNPdbers121918324
MSV3drs121918324
GWAS Ctlgrs121918324
Max Magnitude0
OMIM600923
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121918324(T;T)
Alt rs121918324(T;T)
Reference rs121918324(C;C)
Significance Pathogenic
Disease Variegate porphyria
Variation info
Gene PPOX
CLNDBN Variegate porphyria
Reversed 0
HGVS NC_000001.10:g.161136977C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009233.6,