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rs28934595

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28934595(A;C)
Make rs28934595(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position26091354
GeneHFE
is asnp
is mentioned by
dbSNPrs28934595
ebirs28934595
HLIrs28934595
Exacrs28934595
Varsomers28934595
Maprs28934595
PheGenIrs28934595
hapmaprs28934595
1000 genomesrs28934595
hgdprs28934595
ensemblrs28934595
gopubmedrs28934595
geneviewrs28934595
scholarrs28934595
googlers28934595
pharmgkbrs28934595
gwascentralrs28934595
openSNPrs28934595
23andMers28934595
23andMe allrs28934595
SNP Nexus

SNPshotrs28934595
SNPdbers28934595
MSV3drs28934595
GWAS Ctlgrs28934595
Max Magnitude0
OMIM235200
DescPORPHYRIA VARIEGATA
Variant0007
Relatedalso
Neighborrs28934596
Distance276
OMIM613609
Desc
Variant0007
Relatedalso
Porphyria


ClinVar
Risk rs28934595(C;C)
Alt rs28934595(C;C)
Reference rs28934595(A;A)
Significance Pathogenic
Disease Hemochromatosis type 1
Variation info
Gene HFE
CLNDBN Hemochromatosis type 1
Reversed 0
HGVS NC_000006.11:g.26091582A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000000034.3,