rs796052923

Orientation

minus

Stabilized

minus

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

Make rs796052923(A;A)

Make rs796052923(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

1

Position

40092397

Gene

PPT1

is a	snp
is	mentioned by
dbSNP	rs796052923
dbSNP (classic)	rs796052923
ClinGen	rs796052923
ebi	rs796052923
HLI	rs796052923
Exac	rs796052923
Gnomad	rs796052923
Varsome	rs796052923
LitVar	rs796052923
Map	rs796052923
PheGenI	rs796052923
Biobank	rs796052923
1000 genomes	rs796052923
hgdp	rs796052923
ensembl	rs796052923
geneview	rs796052923
scholar	rs796052923
google	rs796052923
pharmgkb	rs796052923
gwascentral	rs796052923
openSNP	rs796052923
23andMe	rs796052923
SNPshot	rs796052923
SNPdbe	rs796052923
MSV3d	rs796052923
GWAS Ctlg	rs796052923

Max Magnitude

0

ClinVar
Risk	rs796052923(A;A)
Alt	rs796052923(A;A)
Reference	Rs796052923(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PPT1
CLNDBN	not provided
Reversed	1
HGVS	NC_000001.10:g.40558069C>T
CLNSRC
CLNACC	RCV000188710.2,