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rs104894695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894695(C;T)
Make rs104894695(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position35284953
GeneHAMP
is asnp
is mentioned by
dbSNPrs104894695
ebirs104894695
HLIrs104894695
Exacrs104894695
Varsomers104894695
Maprs104894695
PheGenIrs104894695
hapmaprs104894695
1000 genomesrs104894695
hgdprs104894695
ensemblrs104894695
gopubmedrs104894695
geneviewrs104894695
scholarrs104894695
googlers104894695
pharmgkbrs104894695
gwascentralrs104894695
openSNPrs104894695
23andMers104894695
23andMe allrs104894695
SNP Nexus

SNPshotrs104894695
SNPdbers104894695
MSV3drs104894695
GWAS Ctlgrs104894695
Max Magnitude0
OMIM606464
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104894695(T;T)
Alt rs104894695(T;T)
Reference rs104894695(C;C)
Significance Pathogenic
Disease Hemochromatosis type 2B
Variation info
Gene HAMP
CLNDBN Hemochromatosis type 2B
Reversed 0
HGVS NC_000019.9:g.35775856C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004505.2,