rs760977825

Orientation

plus

Stabilized

plus

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

Make rs760977825(C;G)

Make rs760977825(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

62088843

Gene

PIGN

is a	snp
is	mentioned by
dbSNP	rs760977825
dbSNP (classic)	rs760977825
ClinGen	rs760977825
ebi	rs760977825
HLI	rs760977825
Exac	rs760977825
Gnomad	rs760977825
Varsome	rs760977825
LitVar	rs760977825
Map	rs760977825
PheGenI	rs760977825
Biobank	rs760977825
1000 genomes	rs760977825
hgdp	rs760977825
ensembl	rs760977825
geneview	rs760977825
scholar	rs760977825
google	rs760977825
pharmgkb	rs760977825
gwascentral	rs760977825
openSNP	rs760977825
23andMe	rs760977825
SNPshot	rs760977825
SNPdbe	rs760977825
MSV3d	rs760977825
GWAS Ctlg	rs760977825

Max Magnitude

0

ClinVar
Risk	rs760977825(G;G)
Alt	rs760977825(G;G)
Reference	Rs760977825(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PIGN
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.59756076C>G
CLNSRC
CLNACC	RCV000490244.1,