rs1057518061

Orientation

minus

Stabilized

minus

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

Make rs1057518061(C;C)

Make rs1057518061(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

62138238

Gene

PIGN

is a	snp
is	mentioned by
dbSNP	rs1057518061
dbSNP (classic)	rs1057518061
ClinGen	rs1057518061
ebi	rs1057518061
HLI	rs1057518061
Exac	rs1057518061
Gnomad	rs1057518061
Varsome	rs1057518061
LitVar	rs1057518061
Map	rs1057518061
PheGenI	rs1057518061
Biobank	rs1057518061
1000 genomes	rs1057518061
hgdp	rs1057518061
ensembl	rs1057518061
geneview	rs1057518061
scholar	rs1057518061
google	rs1057518061
pharmgkb	rs1057518061
gwascentral	rs1057518061
openSNP	rs1057518061
23andMe	rs1057518061
SNPshot	rs1057518061
SNPdbe	rs1057518061
MSV3d	rs1057518061
GWAS Ctlg	rs1057518061

Max Magnitude

0

ClinVar
Risk	rs1057518061(C;C)
Alt	rs1057518061(C;C)
Reference	Rs1057518061(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	PIGN
CLNDBN	not provided
Reversed	1
HGVS	NC_000018.9:g.59805471C>G
CLNSRC
CLNACC	RCV000413707.1,