rs772153760

Orientation

plus

Stabilized

plus

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

Make rs772153760(C;T)

Make rs772153760(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

55679786

Gene

PNPT1

is a	snp
is	mentioned by
dbSNP	rs772153760
dbSNP (classic)	rs772153760
ClinGen	rs772153760
ebi	rs772153760
HLI	rs772153760
Exac	rs772153760
Gnomad	rs772153760
Varsome	rs772153760
LitVar	rs772153760
Map	rs772153760
PheGenI	rs772153760
Biobank	rs772153760
1000 genomes	rs772153760
hgdp	rs772153760
ensembl	rs772153760
geneview	rs772153760
scholar	rs772153760
google	rs772153760
pharmgkb	rs772153760
gwascentral	rs772153760
openSNP	rs772153760
23andMe	rs772153760
SNPshot	rs772153760
SNPdbe	rs772153760
MSV3d	rs772153760
GWAS Ctlg	rs772153760

Max Magnitude

0

ClinVar
Risk	rs772153760(T;T)
Alt	rs772153760(T;T)
Reference	Rs772153760(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNPT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.55906921C>T
CLNSRC
CLNACC	RCV000195523.2,