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rs767103817

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767103817(A;A)
Make rs767103817(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position119092407
GeneHMBS
is asnp
is mentioned by
dbSNPrs767103817
dbSNP (classic)rs767103817
ClinGenrs767103817
ebirs767103817
HLIrs767103817
Exacrs767103817
Gnomadrs767103817
Varsomers767103817
LitVarrs767103817
Maprs767103817
PheGenIrs767103817
Biobankrs767103817
1000 genomesrs767103817
hgdprs767103817
ensemblrs767103817
geneviewrs767103817
scholarrs767103817
googlers767103817
pharmgkbrs767103817
gwascentralrs767103817
openSNPrs767103817
23andMers767103817
23andMe allrs767103817
SNPshotrs767103817
SNPdbers767103817
MSV3drs767103817
GWAS Ctlgrs767103817
Max Magnitude0
ClinVar
Risk rs767103817(A;A) rs767103817(T;T)
Alt rs767103817(A;A) rs767103817(T;T)
Reference Rs767103817(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HMBS
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118963117G>A
CLNSRC
CLNACC RCV000484759.1,