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rs1057519953

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519953(A;A)
Make rs1057519953(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position49375576
GeneRHOA
is asnp
is mentioned by
dbSNPrs1057519953
dbSNP (old)rs1057519953
ClinGenrs1057519953
ebirs1057519953
HLIrs1057519953
Exacrs1057519953
Gnomadrs1057519953
Varsomers1057519953
Maprs1057519953
PheGenIrs1057519953
Biobankrs1057519953
1000 genomesrs1057519953
hgdprs1057519953
ensemblrs1057519953
gopubmedrs1057519953
geneviewrs1057519953
scholarrs1057519953
googlers1057519953
pharmgkbrs1057519953
gwascentralrs1057519953
openSNPrs1057519953
23andMers1057519953
23andMe allrs1057519953
SNPshotrs1057519953
SNPdbers1057519953
MSV3drs1057519953
GWAS Ctlgrs1057519953
Max Magnitude0
ClinVar
Risk rs1057519953(A;A) rs1057519953(T;T)
Alt rs1057519953(A;A) rs1057519953(T;T)
Reference Rs1057519953(G;G)
Significance Probable-Pathogenic
Disease Malignant lymphoma Oesophageal carcinoma Colorectal Neoplasms Adenocarcinoma of stomach Neoplasm of breast
Variation info
Gene RHOA
CLNDBN Malignant lymphoma, non-Hodgkin Oesophageal carcinoma Colorectal Neoplasms Adenocarcinoma of stomach Neoplasm of breast
Reversed 1
HGVS NC_000003.11:g.49413009C>A; NC_000003.11:g.49413009C>T
CLNSRC
CLNACC RCV000425080.1, RCV000431457.1, RCV000432532.1, RCV000443944.1, RCV000444013.1, RCV000421840.1, RCV000422905.1, RCV000432727.1, RCV000440078.1, RCV000444856.1,