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rs1057519831

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519831(C;T)
Make rs1057519831(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position81912655
GenePLCG2
is asnp
is mentioned by
dbSNPrs1057519831
dbSNP (old)rs1057519831
ClinGenrs1057519831
ebirs1057519831
HLIrs1057519831
Exacrs1057519831
Gnomadrs1057519831
Varsomers1057519831
Maprs1057519831
PheGenIrs1057519831
Biobankrs1057519831
1000 genomesrs1057519831
hgdprs1057519831
ensemblrs1057519831
gopubmedrs1057519831
geneviewrs1057519831
scholarrs1057519831
googlers1057519831
pharmgkbrs1057519831
gwascentralrs1057519831
openSNPrs1057519831
23andMers1057519831
23andMe allrs1057519831
SNPshotrs1057519831
SNPdbers1057519831
MSV3drs1057519831
GWAS Ctlgrs1057519831
Max Magnitude0
ClinVar
Risk rs1057519831(T;T)
Alt rs1057519831(T;T)
Reference Rs1057519831(C;C)
Significance Probable-Pathogenic
Disease Chronic lymphocytic leukemia
Variation info
Gene PLCG2
CLNDBN Chronic lymphocytic leukemia
Reversed 0
HGVS NC_000016.9:g.81946260C>T
CLNSRC
CLNACC RCV000443129.1,