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rs1057519912

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519912(C;T)
Make rs1057519912(T;T)
ReferenceGRCh38.p7 38.3/150
ChromosomeX
Position71129408
GeneMED12
is asnp
is mentioned by
dbSNPrs1057519912
dbSNP (old)rs1057519912
ClinGenrs1057519912
ebirs1057519912
HLIrs1057519912
Exacrs1057519912
Gnomadrs1057519912
Varsomers1057519912
LitVarrs1057519912
Maprs1057519912
PheGenIrs1057519912
Biobankrs1057519912
1000 genomesrs1057519912
hgdprs1057519912
ensemblrs1057519912
gopubmedrs1057519912
geneviewrs1057519912
scholarrs1057519912
googlers1057519912
pharmgkbrs1057519912
gwascentralrs1057519912
openSNPrs1057519912
23andMers1057519912
23andMe allrs1057519912
SNPshotrs1057519912
SNPdbers1057519912
MSV3drs1057519912
GWAS Ctlgrs1057519912
Max Magnitude0
ClinVar
Risk rs1057519912(G;G) rs1057519912(T;T)
Alt rs1057519912(G;G) rs1057519912(T;T)
Reference Rs1057519912(C;C)
Significance Probable-Pathogenic
Disease Adenocarcinoma of prostate Squamous cell carcinoma of lung Adenocarcinoma of stomach Neoplasm of breast Pancreatic adenocarcinoma
Variation info
Gene MED12
CLNDBN Adenocarcinoma of prostate Squamous cell carcinoma of lung Adenocarcinoma of stomach Neoplasm of breast Pancreatic adenocarcinoma
Reversed 0
HGVS NC_000023.10:g.70349258C>G; NC_000023.10:g.70349258C>T
CLNSRC
CLNACC RCV000417890.1, RCV000418945.1, RCV000424408.1, RCV000428595.1, RCV000435099.1, RCV000425461.1, RCV000426762.1, RCV000433808.1, RCV000436162.1, RCV000445331.1,