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rs1057519853

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs1057519853(CA;TT)
Make rs1057519853(TT;TT)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position77794572
GeneGNAQ
is asnp
is mentioned by
dbSNPrs1057519853
dbSNP (old)rs1057519853
ClinGenrs1057519853
ebirs1057519853
HLIrs1057519853
Exacrs1057519853
Gnomadrs1057519853
Varsomers1057519853
Maprs1057519853
PheGenIrs1057519853
Biobankrs1057519853
1000 genomesrs1057519853
hgdprs1057519853
ensemblrs1057519853
gopubmedrs1057519853
geneviewrs1057519853
scholarrs1057519853
googlers1057519853
pharmgkbrs1057519853
gwascentralrs1057519853
openSNPrs1057519853
23andMers1057519853
23andMe allrs1057519853
SNPshotrs1057519853
SNPdbers1057519853
MSV3drs1057519853
GWAS Ctlgrs1057519853
Max Magnitude0
ClinVar
Risk rs1057519853(TT;TT)
Alt rs1057519853(TT;TT)
Reference Rs1057519853(CA;CA)
Significance Probable-Pathogenic
Disease Intraocular melanoma
Variation info
Gene GNAQ
CLNDBN Intraocular melanoma
Reversed 1
HGVS NC_000009.11:g.80409488_80409489delTGinsAA
CLNSRC
CLNACC RCV000441114.1,