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rs1057519742

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519742(A;C)
Make rs1057519742(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position3118944
GeneGNA11
is asnp
is mentioned by
dbSNPrs1057519742
dbSNP (old)rs1057519742
ClinGenrs1057519742
ebirs1057519742
HLIrs1057519742
Exacrs1057519742
Gnomadrs1057519742
Varsomers1057519742
Maprs1057519742
PheGenIrs1057519742
Biobankrs1057519742
1000 genomesrs1057519742
hgdprs1057519742
ensemblrs1057519742
gopubmedrs1057519742
geneviewrs1057519742
scholarrs1057519742
googlers1057519742
pharmgkbrs1057519742
gwascentralrs1057519742
openSNPrs1057519742
23andMers1057519742
23andMe allrs1057519742
SNPshotrs1057519742
SNPdbers1057519742
MSV3drs1057519742
GWAS Ctlgrs1057519742
Max Magnitude0
ClinVar
Risk rs1057519742(C;C) rs1057519742(T;T)
Alt rs1057519742(C;C) rs1057519742(T;T)
Reference Rs1057519742(A;A)
Significance Pathogenic
Disease Malignant melanoma Intraocular melanoma Malignant melanoma of skin
Variation info
Gene GNA11
CLNDBN Malignant melanoma Intraocular melanoma Malignant melanoma of skin
Reversed 0
HGVS NC_000019.9:g.3118942A>C; NC_000019.9:g.3118942A>T
CLNSRC
CLNACC RCV000425941.1, RCV000432719.1, RCV000425425.1, RCV000437415.1, RCV000444127.1,