rs767310806

Orientation

plus

Stabilized

plus

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

Make rs767310806(G;G)

Make rs767310806(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

55654942

Gene

PNPT1

is a	snp
is	mentioned by
dbSNP	rs767310806
dbSNP (classic)	rs767310806
ClinGen	rs767310806
ebi	rs767310806
HLI	rs767310806
Exac	rs767310806
Gnomad	rs767310806
Varsome	rs767310806
LitVar	rs767310806
Map	rs767310806
PheGenI	rs767310806
Biobank	rs767310806
1000 genomes	rs767310806
hgdp	rs767310806
ensembl	rs767310806
geneview	rs767310806
scholar	rs767310806
google	rs767310806
pharmgkb	rs767310806
gwascentral	rs767310806
openSNP	rs767310806
23andMe	rs767310806
SNPshot	rs767310806
SNPdbe	rs767310806
MSV3d	rs767310806
GWAS Ctlg	rs767310806

Max Magnitude

0

ClinVar
Risk	rs767310806(C;C) rs767310806(G;G)
Alt	rs767310806(C;C) rs767310806(G;G)
Reference	Rs767310806(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNPT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.55882077T>C
CLNSRC
CLNACC	RCV000195745.2,