rs863224168

Orientation

minus

Stabilized

minus

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

Make rs863224168(C;C)

Make rs863224168(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

55684996

Gene

PNPT1

is a	snp
is	mentioned by
dbSNP	rs863224168
dbSNP (classic)	rs863224168
ClinGen	rs863224168
ebi	rs863224168
HLI	rs863224168
Exac	rs863224168
Gnomad	rs863224168
Varsome	rs863224168
LitVar	rs863224168
Map	rs863224168
PheGenI	rs863224168
Biobank	rs863224168
1000 genomes	rs863224168
hgdp	rs863224168
ensembl	rs863224168
geneview	rs863224168
scholar	rs863224168
google	rs863224168
pharmgkb	rs863224168
gwascentral	rs863224168
openSNP	rs863224168
23andMe	rs863224168
SNPshot	rs863224168
SNPdbe	rs863224168
MSV3d	rs863224168
GWAS Ctlg	rs863224168

Max Magnitude

0

ClinVar
Risk	rs863224168(C;C)
Alt	rs863224168(C;C)
Reference	Rs863224168(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PNPT1
CLNDBN	not provided
Reversed	1
HGVS	NC_000002.11:g.55912131A>G
CLNSRC
CLNACC	RCV000196562.1,