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rs1057518032

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518032(A;A)
Make rs1057518032(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position74774617
GeneFA2H
is asnp
is mentioned by
dbSNPrs1057518032
dbSNP (old)rs1057518032
ClinGenrs1057518032
ebirs1057518032
HLIrs1057518032
Exacrs1057518032
Gnomadrs1057518032
Varsomers1057518032
Maprs1057518032
PheGenIrs1057518032
Biobankrs1057518032
1000 genomesrs1057518032
hgdprs1057518032
ensemblrs1057518032
gopubmedrs1057518032
geneviewrs1057518032
scholarrs1057518032
googlers1057518032
pharmgkbrs1057518032
gwascentralrs1057518032
openSNPrs1057518032
23andMers1057518032
23andMe allrs1057518032
SNPshotrs1057518032
SNPdbers1057518032
MSV3drs1057518032
GWAS Ctlgrs1057518032
Max Magnitude0
ClinVar
Risk rs1057518032(A;A)
Alt rs1057518032(A;A)
Reference Rs1057518032(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FA2H
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.74808515C>T
CLNSRC
CLNACC RCV000413571.1,