rs1057519832

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1057519832(A;C)

Make rs1057519832(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

81928578

Gene

PLCG2

is a	snp
is	mentioned by
dbSNP	rs1057519832
dbSNP (classic)	rs1057519832
ClinGen	rs1057519832
ebi	rs1057519832
HLI	rs1057519832
Exac	rs1057519832
Gnomad	rs1057519832
Varsome	rs1057519832
LitVar	rs1057519832
Map	rs1057519832
PheGenI	rs1057519832
Biobank	rs1057519832
1000 genomes	rs1057519832
hgdp	rs1057519832
ensembl	rs1057519832
geneview	rs1057519832
scholar	rs1057519832
google	rs1057519832
pharmgkb	rs1057519832
gwascentral	rs1057519832
openSNP	rs1057519832
23andMe	rs1057519832
SNPshot	rs1057519832
SNPdbe	rs1057519832
MSV3d	rs1057519832
GWAS Ctlg	rs1057519832

Max Magnitude

0

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,