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rs1057524810

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524810(A;A)
Make rs1057524810(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position30691505
GeneTGFBR2
is asnp
is mentioned by
dbSNPrs1057524810
dbSNP (old)rs1057524810
ClinGenrs1057524810
ebirs1057524810
HLIrs1057524810
Exacrs1057524810
Gnomadrs1057524810
Varsomers1057524810
Maprs1057524810
PheGenIrs1057524810
Biobankrs1057524810
1000 genomesrs1057524810
hgdprs1057524810
ensemblrs1057524810
gopubmedrs1057524810
geneviewrs1057524810
scholarrs1057524810
googlers1057524810
pharmgkbrs1057524810
gwascentralrs1057524810
openSNPrs1057524810
23andMers1057524810
23andMe allrs1057524810
SNPshotrs1057524810
SNPdbers1057524810
MSV3drs1057524810
GWAS Ctlgrs1057524810
Max Magnitude0
ClinVar
Risk rs1057524810(A;A)
Alt rs1057524810(A;A)
Reference Rs1057524810(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TGFBR2
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.30732997G>A
CLNSRC
CLNACC RCV000429672.1,