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rs1057519952

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519952(C;T)
Make rs1057519952(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position49375577
GeneRHOA
is asnp
is mentioned by
dbSNPrs1057519952
dbSNP (classic)rs1057519952
ClinGenrs1057519952
ebirs1057519952
HLIrs1057519952
Exacrs1057519952
Gnomadrs1057519952
Varsomers1057519952
LitVarrs1057519952
Maprs1057519952
PheGenIrs1057519952
Biobankrs1057519952
1000 genomesrs1057519952
hgdprs1057519952
ensemblrs1057519952
geneviewrs1057519952
scholarrs1057519952
googlers1057519952
pharmgkbrs1057519952
gwascentralrs1057519952
openSNPrs1057519952
23andMers1057519952
23andMe allrs1057519952
SNPshotrs1057519952
SNPdbers1057519952
MSV3drs1057519952
GWAS Ctlgrs1057519952
Max Magnitude0
ClinVar
Risk rs1057519952(T;T)
Alt rs1057519952(T;T)
Reference Rs1057519952(C;C)
Significance Probable-Pathogenic
Disease Oesophageal carcinoma Malignant lymphoma Adenocarcinoma of stomach Neoplasm of breast Colorectal Neoplasms
Variation info
Gene RHOA
CLNDBN Oesophageal carcinoma Malignant lymphoma, non-Hodgkin Adenocarcinoma of stomach Neoplasm of breast Colorectal Neoplasms
Reversed 1
HGVS NC_000003.11:g.49413010G>A
CLNSRC
CLNACC RCV000420653.1, RCV000423113.1, RCV000430318.1, RCV000430517.1, RCV000441218.1,