rs1060499765

Orientation

plus

Stabilized

plus

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

Make rs1060499765(A;A)

Make rs1060499765(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

20

Position

8737163

Gene

PLCB1

is a	snp
is	mentioned by
dbSNP	rs1060499765
dbSNP (classic)	rs1060499765
ClinGen	rs1060499765
ebi	rs1060499765
HLI	rs1060499765
Exac	rs1060499765
Gnomad	rs1060499765
Varsome	rs1060499765
LitVar	rs1060499765
Map	rs1060499765
PheGenI	rs1060499765
Biobank	rs1060499765
1000 genomes	rs1060499765
hgdp	rs1060499765
ensembl	rs1060499765
geneview	rs1060499765
scholar	rs1060499765
google	rs1060499765
pharmgkb	rs1060499765
gwascentral	rs1060499765
openSNP	rs1060499765
23andMe	rs1060499765
SNPshot	rs1060499765
SNPdbe	rs1060499765
MSV3d	rs1060499765
GWAS Ctlg	rs1060499765

Max Magnitude

0

ClinVar
Risk	rs1060499765(A;A)
Alt	rs1060499765(A;A)
Reference	Rs1060499765(T;T)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	PLCB1
CLNDBN	Abnormality of brain morphology
Reversed	0
HGVS	NC_000020.10:g.8717810T>A
CLNSRC
CLNACC	RCV000454325.1,