rs1057519831

Orientation

plus

Stabilized

plus

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

Make rs1057519831(C;T)

Make rs1057519831(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

81912655

Gene

PLCG2

is a	snp
is	mentioned by
dbSNP	rs1057519831
dbSNP (classic)	rs1057519831
ClinGen	rs1057519831
ebi	rs1057519831
HLI	rs1057519831
Exac	rs1057519831
Gnomad	rs1057519831
Varsome	rs1057519831
LitVar	rs1057519831
Map	rs1057519831
PheGenI	rs1057519831
Biobank	rs1057519831
1000 genomes	rs1057519831
hgdp	rs1057519831
ensembl	rs1057519831
geneview	rs1057519831
scholar	rs1057519831
google	rs1057519831
pharmgkb	rs1057519831
gwascentral	rs1057519831
openSNP	rs1057519831
23andMe	rs1057519831
SNPshot	rs1057519831
SNPdbe	rs1057519831
MSV3d	rs1057519831
GWAS Ctlg	rs1057519831

Max Magnitude

0

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,