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rs1057521126

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521126(A;A)
Make rs1057521126(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position119092785
GeneHMBS
is asnp
is mentioned by
dbSNPrs1057521126
dbSNP (old)rs1057521126
ClinGenrs1057521126
ebirs1057521126
HLIrs1057521126
Exacrs1057521126
Gnomadrs1057521126
Varsomers1057521126
Maprs1057521126
PheGenIrs1057521126
Biobankrs1057521126
1000 genomesrs1057521126
hgdprs1057521126
ensemblrs1057521126
gopubmedrs1057521126
geneviewrs1057521126
scholarrs1057521126
googlers1057521126
pharmgkbrs1057521126
gwascentralrs1057521126
openSNPrs1057521126
23andMers1057521126
23andMe allrs1057521126
SNPshotrs1057521126
SNPdbers1057521126
MSV3drs1057521126
GWAS Ctlgrs1057521126
Max Magnitude0
ClinVar
Risk rs1057521126(A;A)
Alt rs1057521126(A;A)
Reference Rs1057521126(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene HMBS
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.118963495G>A
CLNSRC
CLNACC RCV000430573.1,