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rs74315323

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs74315323(G;T)
Make rs74315323(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position146018399
GeneHFE2
is asnp
is mentioned by
dbSNPrs74315323
ebirs74315323
HLIrs74315323
Exacrs74315323
Varsomers74315323
Maprs74315323
PheGenIrs74315323
hapmaprs74315323
1000 genomesrs74315323
hgdprs74315323
ensemblrs74315323
gopubmedrs74315323
geneviewrs74315323
scholarrs74315323
googlers74315323
pharmgkbrs74315323
gwascentralrs74315323
openSNPrs74315323
23andMers74315323
23andMe allrs74315323
SNP Nexus

SNPshotrs74315323
SNPdbers74315323
MSV3drs74315323
GWAS Ctlgrs74315323
Max Magnitude0
OMIM608374
Desc
Variant0001
Relatedalso
ClinVar
Risk rs74315323(T;T)
Alt rs74315323(T;T)
Reference rs74315323(G;G)
Significance Pathogenic
Disease Hemochromatosis type 2A Hemochromatosis type 1
Variation info
Gene HFE2
CLNDBN Hemochromatosis type 2A Hemochromatosis type 1
Reversed 0
HGVS NC_000001.10:g.145416614G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000002461.4, RCV000002462.3,