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rs1057519951

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519951(C;C)
Make rs1057519951(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position49375472
GeneRHOA
is asnp
is mentioned by
dbSNPrs1057519951
dbSNP (old)rs1057519951
ClinGenrs1057519951
ebirs1057519951
HLIrs1057519951
Exacrs1057519951
Gnomadrs1057519951
Varsomers1057519951
Maprs1057519951
PheGenIrs1057519951
Biobankrs1057519951
1000 genomesrs1057519951
hgdprs1057519951
ensemblrs1057519951
gopubmedrs1057519951
geneviewrs1057519951
scholarrs1057519951
googlers1057519951
pharmgkbrs1057519951
gwascentralrs1057519951
openSNPrs1057519951
23andMers1057519951
23andMe allrs1057519951
SNPshotrs1057519951
SNPdbers1057519951
MSV3drs1057519951
GWAS Ctlgrs1057519951
Max Magnitude0
ClinVar
Risk rs1057519951(A;A) rs1057519951(C;C)
Alt rs1057519951(A;A) rs1057519951(C;C)
Reference Rs1057519951(G;G)
Significance Probable-Pathogenic
Disease Neoplasm of breast Adenocarcinoma of lung Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck
Variation info
Gene RHOA
CLNDBN Neoplasm of breast Adenocarcinoma of lung Adenocarcinoma of stomach Squamous cell carcinoma of the head and neck
Reversed 1
HGVS NC_000003.11:g.49412905C>G; NC_000003.11:g.49412905C>T
CLNSRC
CLNACC RCV000425677.1, RCV000425897.1, RCV000436482.1, RCV000443212.1, RCV000418248.1, RCV000428054.1, RCV000435238.1, RCV000435482.1,