rs764567774

Orientation

plus

Stabilized

plus

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

Make rs764567774(-;-)

Make rs764567774(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

44065510

Gene

PGAM2

is a	snp
is	mentioned by
dbSNP	rs764567774
dbSNP (classic)	rs764567774
ClinGen	rs764567774
ebi	rs764567774
HLI	rs764567774
Exac	rs764567774
Gnomad	rs764567774
Varsome	rs764567774
LitVar	rs764567774
Map	rs764567774
PheGenI	rs764567774
Biobank	rs764567774
1000 genomes	rs764567774
hgdp	rs764567774
ensembl	rs764567774
geneview	rs764567774
scholar	rs764567774
google	rs764567774
pharmgkb	rs764567774
gwascentral	rs764567774
openSNP	rs764567774
23andMe	rs764567774
SNPshot	rs764567774
SNPdbe	rs764567774
MSV3d	rs764567774
GWAS Ctlg	rs764567774

Max Magnitude

0

ClinVar
Risk	rs764567774(-;-)
Alt	rs764567774(-;-)
Reference	Rs764567774(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PGAM2
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.44105109delA
CLNSRC
CLNACC	RCV000489223.1,