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rs1057517972

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517972(A;G)
Make rs1057517972(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position80153055
GeneFAH
is asnp
is mentioned by
dbSNPrs1057517972
dbSNP (old)rs1057517972
ClinGenrs1057517972
ebirs1057517972
HLIrs1057517972
Exacrs1057517972
Gnomadrs1057517972
Varsomers1057517972
Maprs1057517972
PheGenIrs1057517972
Biobankrs1057517972
1000 genomesrs1057517972
hgdprs1057517972
ensemblrs1057517972
gopubmedrs1057517972
geneviewrs1057517972
scholarrs1057517972
googlers1057517972
pharmgkbrs1057517972
gwascentralrs1057517972
openSNPrs1057517972
23andMers1057517972
23andMe allrs1057517972
SNPshotrs1057517972
SNPdbers1057517972
MSV3drs1057517972
GWAS Ctlgrs1057517972
Max Magnitude0
ClinVar
Risk rs1057517972(G;G)
Alt rs1057517972(G;G)
Reference Rs1057517972(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FAH
CLNDBN not provided
Reversed 0
HGVS NC_000015.9:g.80445397A>G
CLNSRC
CLNACC RCV000414667.1,