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rs1057518477

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518477(A;G)
Make rs1057518477(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position120840111
GeneTSPAN12
is asnp
is mentioned by
dbSNPrs1057518477
dbSNP (old)rs1057518477
ClinGenrs1057518477
ebirs1057518477
HLIrs1057518477
Exacrs1057518477
Gnomadrs1057518477
Varsomers1057518477
Maprs1057518477
PheGenIrs1057518477
Biobankrs1057518477
1000 genomesrs1057518477
hgdprs1057518477
ensemblrs1057518477
gopubmedrs1057518477
geneviewrs1057518477
scholarrs1057518477
googlers1057518477
pharmgkbrs1057518477
gwascentralrs1057518477
openSNPrs1057518477
23andMers1057518477
23andMe allrs1057518477
SNPshotrs1057518477
SNPdbers1057518477
MSV3drs1057518477
GWAS Ctlgrs1057518477
Max Magnitude0
ClinVar
Risk rs1057518477(G;G)
Alt rs1057518477(G;G)
Reference Rs1057518477(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TSPAN12
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.120480165T>C
CLNSRC
CLNACC RCV000413300.1,