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rs387906549

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906549(A;T)
Make rs387906549(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position61967589
GeneFTH1
is asnp
is mentioned by
dbSNPrs387906549
ebirs387906549
HLIrs387906549
Exacrs387906549
Varsomers387906549
Maprs387906549
PheGenIrs387906549
hapmaprs387906549
1000 genomesrs387906549
hgdprs387906549
ensemblrs387906549
gopubmedrs387906549
geneviewrs387906549
scholarrs387906549
googlers387906549
pharmgkbrs387906549
gwascentralrs387906549
openSNPrs387906549
23andMers387906549
23andMe allrs387906549
SNP Nexus

SNPshotrs387906549
SNPdbers387906549
MSV3drs387906549
GWAS Ctlgrs387906549
Max Magnitude0
ClinVar
Risk rs387906549(T;T)
Alt rs387906549(T;T)
Reference rs387906549(A;A)
Significance Pathogenic
Disease Hemochromatosis type 5
Variation info
Gene FTH1 LOC399900
CLNDBN Hemochromatosis type 5
Reversed 1
HGVS NC_000011.9:g.61735061T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000017954.32,