rs746882521

Orientation

plus

Stabilized

plus

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

Make rs746882521(A;C)

Make rs746882521(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

62143337

Gene

PIGN

is a	snp
is	mentioned by
dbSNP	rs746882521
dbSNP (classic)	rs746882521
ClinGen	rs746882521
ebi	rs746882521
HLI	rs746882521
Exac	rs746882521
Gnomad	rs746882521
Varsome	rs746882521
LitVar	rs746882521
Map	rs746882521
PheGenI	rs746882521
Biobank	rs746882521
1000 genomes	rs746882521
hgdp	rs746882521
ensembl	rs746882521
geneview	rs746882521
scholar	rs746882521
google	rs746882521
pharmgkb	rs746882521
gwascentral	rs746882521
openSNP	rs746882521
23andMe	rs746882521
SNPshot	rs746882521
SNPdbe	rs746882521
MSV3d	rs746882521
GWAS Ctlg	rs746882521

Max Magnitude

0

ClinVar
Risk	rs746882521(C;C)
Alt	rs746882521(C;C)
Reference	Rs746882521(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PIGN
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.59810570A>C
CLNSRC
CLNACC	RCV000489201.1,