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rs1057519880

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519880(A;A)
Make rs1057519880(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position49665875
GeneBCL2L12, IRF3
is asnp
is mentioned by
dbSNPrs1057519880
dbSNP (old)rs1057519880
ClinGenrs1057519880
ebirs1057519880
HLIrs1057519880
Exacrs1057519880
Gnomadrs1057519880
Varsomers1057519880
LitVarrs1057519880
Maprs1057519880
PheGenIrs1057519880
Biobankrs1057519880
1000 genomesrs1057519880
hgdprs1057519880
ensemblrs1057519880
gopubmedrs1057519880
geneviewrs1057519880
scholarrs1057519880
googlers1057519880
pharmgkbrs1057519880
gwascentralrs1057519880
openSNPrs1057519880
23andMers1057519880
23andMe allrs1057519880
SNPshotrs1057519880
SNPdbers1057519880
MSV3drs1057519880
GWAS Ctlgrs1057519880
Max Magnitude0
ClinVar
Risk rs1057519880(A;A)
Alt rs1057519880(A;A)
Reference Rs1057519880(G;G)
Significance Probable-Pathogenic
Disease Malignant melanoma of skin Squamous cell carcinoma of the skin
Variation info
Gene BCL2L12 IRF3
CLNDBN Malignant melanoma of skin Squamous cell carcinoma of the skin
Reversed 1
HGVS NC_000019.9:g.50169132C>T
CLNSRC
CLNACC RCV000426971.1, RCV000442298.1,