rs773629540

Orientation

plus

Stabilized

plus

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

Make rs773629540(A;A)

Make rs773629540(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

62148326

Gene

PIGN

is a	snp
is	mentioned by
dbSNP	rs773629540
dbSNP (classic)	rs773629540
ClinGen	rs773629540
ebi	rs773629540
HLI	rs773629540
Exac	rs773629540
Gnomad	rs773629540
Varsome	rs773629540
LitVar	rs773629540
Map	rs773629540
PheGenI	rs773629540
Biobank	rs773629540
1000 genomes	rs773629540
hgdp	rs773629540
ensembl	rs773629540
geneview	rs773629540
scholar	rs773629540
google	rs773629540
pharmgkb	rs773629540
gwascentral	rs773629540
openSNP	rs773629540
23andMe	rs773629540
SNPshot	rs773629540
SNPdbe	rs773629540
MSV3d	rs773629540
GWAS Ctlg	rs773629540

Max Magnitude

0

ClinVar
Risk	rs773629540(A;A)
Alt	rs773629540(A;A)
Reference	Rs773629540(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PIGN
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.59815559G>A
CLNSRC
CLNACC	RCV000481779.1,