rs774425075

Orientation

plus

Stabilized

plus

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

Make rs774425075(C;T)

Make rs774425075(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

55680855

Gene

PNPT1

is a	snp
is	mentioned by
dbSNP	rs774425075
dbSNP (classic)	rs774425075
ClinGen	rs774425075
ebi	rs774425075
HLI	rs774425075
Exac	rs774425075
Gnomad	rs774425075
Varsome	rs774425075
LitVar	rs774425075
Map	rs774425075
PheGenI	rs774425075
Biobank	rs774425075
1000 genomes	rs774425075
hgdp	rs774425075
ensembl	rs774425075
geneview	rs774425075
scholar	rs774425075
google	rs774425075
pharmgkb	rs774425075
gwascentral	rs774425075
openSNP	rs774425075
23andMe	rs774425075
SNPshot	rs774425075
SNPdbe	rs774425075
MSV3d	rs774425075
GWAS Ctlg	rs774425075

Max Magnitude

0

ClinVar
Risk	rs774425075(T;T)
Alt	rs774425075(T;T)
Reference	Rs774425075(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNPT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.55907990C>T
CLNSRC
CLNACC	RCV000489241.1,