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rs104894696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894696(A;A)
Make rs104894696(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position35284999
GeneHAMP
is asnp
is mentioned by
dbSNPrs104894696
ebirs104894696
HLIrs104894696
Exacrs104894696
Varsomers104894696
Maprs104894696
PheGenIrs104894696
hapmaprs104894696
1000 genomesrs104894696
hgdprs104894696
ensemblrs104894696
gopubmedrs104894696
geneviewrs104894696
scholarrs104894696
googlers104894696
pharmgkbrs104894696
gwascentralrs104894696
openSNPrs104894696
23andMers104894696
23andMe allrs104894696
SNP Nexus

SNPshotrs104894696
SNPdbers104894696
MSV3drs104894696
GWAS Ctlgrs104894696
GMAF0.0004591
Max Magnitude0
OMIM606464
Desc
Variant0004
Relatedalso
ClinVar
Risk rs104894696(A;A)
Alt rs104894696(A;A)
Reference rs104894696(G;G)
Significance Other
Disease Hemochromatosis Hemochromatosis type 1
Variation info
Gene HAMP
CLNDBN Hemochromatosis, type 2a, modifier of Hemochromatosis type 1
Reversed 0
HGVS NC_000019.9:g.35775902G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004507.3, RCV000205666.2,