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rs1057519832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519832(A;C)
Make rs1057519832(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position81928578
GenePLCG2
is asnp
is mentioned by
dbSNPrs1057519832
dbSNP (old)rs1057519832
ClinGenrs1057519832
ebirs1057519832
HLIrs1057519832
Exacrs1057519832
Gnomadrs1057519832
Varsomers1057519832
Maprs1057519832
PheGenIrs1057519832
Biobankrs1057519832
1000 genomesrs1057519832
hgdprs1057519832
ensemblrs1057519832
gopubmedrs1057519832
geneviewrs1057519832
scholarrs1057519832
googlers1057519832
pharmgkbrs1057519832
gwascentralrs1057519832
openSNPrs1057519832
23andMers1057519832
23andMe allrs1057519832
SNPshotrs1057519832
SNPdbers1057519832
MSV3drs1057519832
GWAS Ctlgrs1057519832
Max Magnitude0
ClinVar
Risk rs1057519832(C;C) rs1057519832(T;T)
Alt rs1057519832(C;C) rs1057519832(T;T)
Reference Rs1057519832(A;A)
Significance Probable-Pathogenic
Disease Chronic lymphocytic leukemia
Variation info
Gene PLCG2
CLNDBN Chronic lymphocytic leukemia
Reversed 0
HGVS NC_000016.9:g.81962183A>C; NC_000016.9:g.81962183A>T
CLNSRC
CLNACC RCV000426878.1, RCV000435800.1,