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rs763369315

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs763369315(C;T)
Make rs763369315(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position35285003
GeneHAMP
is asnp
is mentioned by
dbSNPrs763369315
ebirs763369315
HLIrs763369315
Exacrs763369315
Varsomers763369315
Maprs763369315
PheGenIrs763369315
hapmaprs763369315
1000 genomesrs763369315
hgdprs763369315
ensemblrs763369315
gopubmedrs763369315
geneviewrs763369315
scholarrs763369315
googlers763369315
pharmgkbrs763369315
gwascentralrs763369315
openSNPrs763369315
23andMers763369315
23andMe allrs763369315
SNP Nexus

SNPshotrs763369315
SNPdbers763369315
MSV3drs763369315
GWAS Ctlgrs763369315
Max Magnitude0
ClinVar
Risk rs763369315(A,T;A,T)
Alt rs763369315(A,T;A,T)
Reference rs763369315(C;C)
Significance Pathogenic
Disease Hemochromatosis type 1
Variation info
Gene HAMP
CLNDBN Hemochromatosis type 1
Reversed 0
HGVS NC_000019.9:g.35775906C>A
CLNSRC
CLNACC RCV000167903.1,