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rs1057519947

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519947(A;A)
Make rs1057519947(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position52212730
GenePPP2R1A
is asnp
is mentioned by
dbSNPrs1057519947
dbSNP (old)rs1057519947
ClinGenrs1057519947
ebirs1057519947
HLIrs1057519947
Exacrs1057519947
Gnomadrs1057519947
Varsomers1057519947
Maprs1057519947
PheGenIrs1057519947
Biobankrs1057519947
1000 genomesrs1057519947
hgdprs1057519947
ensemblrs1057519947
gopubmedrs1057519947
geneviewrs1057519947
scholarrs1057519947
googlers1057519947
pharmgkbrs1057519947
gwascentralrs1057519947
openSNPrs1057519947
23andMers1057519947
23andMe allrs1057519947
SNPshotrs1057519947
SNPdbers1057519947
MSV3drs1057519947
GWAS Ctlgrs1057519947
Max Magnitude0
ClinVar
Risk rs1057519947(A;A)
Alt rs1057519947(A;A)
Reference Rs1057519947(G;G)
Significance Probable-Pathogenic
Disease Uterine Carcinosarcoma Colorectal Neoplasms Adenocarcinoma of lung Malignant neoplasm of body of uterus Neoplasm of breast Adenocarcinoma of stomach Adenocarcinoma of prostate Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma
Variation info
Gene PPP2R1A
CLNDBN Uterine Carcinosarcoma Colorectal Neoplasms Adenocarcinoma of lung Malignant neoplasm of body of uterus Neoplasm of breast Adenocarcinoma of stomach Adenocarcinoma of prostate Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma
Reversed 0
HGVS NC_000019.9:g.52715983G>A
CLNSRC
CLNACC RCV000420373.1, RCV000422450.1, RCV000423122.1, RCV000430627.1, RCV000432728.1, RCV000433386.1, RCV000440118.1, RCV000440878.1, RCV000444029.1,