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rs34413634

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs34413634(C;T)
Make rs34413634(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position119091497
GeneHMBS
is asnp
is mentioned by
dbSNPrs34413634
ebirs34413634
HLIrs34413634
Exacrs34413634
Varsomers34413634
Maprs34413634
PheGenIrs34413634
hapmaprs34413634
1000 genomesrs34413634
hgdprs34413634
ensemblrs34413634
gopubmedrs34413634
geneviewrs34413634
scholarrs34413634
googlers34413634
pharmgkbrs34413634
gwascentralrs34413634
openSNPrs34413634
23andMers34413634
23andMe allrs34413634
SNP Nexus

SNPshotrs34413634
SNPdbers34413634
MSV3drs34413634
GWAS Ctlgrs34413634
Max Magnitude0
ClinVar
Risk rs34413634(T;T)
Alt rs34413634(T;T)
Reference rs34413634(C;C)
Significance Probable-Pathogenic
Disease Acute intermittent porphyria
Variation info
Gene HMBS
CLNDBN Acute intermittent porphyria
Reversed 0
HGVS NC_000011.9:g.118962207C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000148509.1,