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rs1057518208

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518208(A;A)
Make rs1057518208(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position39011657
GeneADAM9
is asnp
is mentioned by
dbSNPrs1057518208
dbSNP (old)rs1057518208
ClinGenrs1057518208
ebirs1057518208
HLIrs1057518208
Exacrs1057518208
Gnomadrs1057518208
Varsomers1057518208
Maprs1057518208
PheGenIrs1057518208
Biobankrs1057518208
1000 genomesrs1057518208
hgdprs1057518208
ensemblrs1057518208
gopubmedrs1057518208
geneviewrs1057518208
scholarrs1057518208
googlers1057518208
pharmgkbrs1057518208
gwascentralrs1057518208
openSNPrs1057518208
23andMers1057518208
23andMe allrs1057518208
SNPshotrs1057518208
SNPdbers1057518208
MSV3drs1057518208
GWAS Ctlgrs1057518208
Max Magnitude0
ClinVar
Risk rs1057518208(A;A)
Alt rs1057518208(A;A)
Reference Rs1057518208(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ADAM9
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.38869176G>A
CLNSRC
CLNACC RCV000413336.1,