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rs1057519941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519941(G;G)
Make rs1057519941(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position179203761
GenePIK3CA
is asnp
is mentioned by
dbSNPrs1057519941
dbSNP (classic)rs1057519941
ClinGenrs1057519941
ebirs1057519941
HLIrs1057519941
Exacrs1057519941
Gnomadrs1057519941
Varsomers1057519941
LitVarrs1057519941
Maprs1057519941
PheGenIrs1057519941
Biobankrs1057519941
1000 genomesrs1057519941
hgdprs1057519941
ensemblrs1057519941
geneviewrs1057519941
scholarrs1057519941
googlers1057519941
pharmgkbrs1057519941
gwascentralrs1057519941
openSNPrs1057519941
23andMers1057519941
SNPshotrs1057519941
SNPdbers1057519941
MSV3drs1057519941
GWAS Ctlgrs1057519941
Max Magnitude0
ClinVar
Risk rs1057519941(C;C) rs1057519941(G;G)
Alt rs1057519941(C;C) rs1057519941(G;G)
Reference Rs1057519941(T;T)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Glioblastoma Uterine cervical neoplasms Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Malignant lymphoma Colorectal Neoplasms Neoplasm of breast
Variation info
Gene PIK3CA
CLNDBN Malignant melanoma of skin Glioblastoma Uterine cervical neoplasms Squamous cell carcinoma of the head and neck Malignant neoplasm of body of uterus Malignant lymphoma, non-Hodgkin Colorectal Neoplasms Neoplasm of breast
Reversed 0
HGVS NC_000003.11:g.178921549T>C; NC_000003.11:g.178921549T>G
CLNSRC
CLNACC RCV000417995.1, RCV000419612.1, RCV000424496.1, RCV000428687.1, RCV000429893.1, RCV000435208.1, RCV000435882.1, RCV000440109.1, RCV000417650.1, RCV000421854.1, RCV000422522.1, RCV000428317.1, RCV000429042.1, RCV000438355.1, RCV000438998.1, RCV000439748.1,