rs1060499763

Orientation

minus

Stabilized

minus

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

Make rs1060499763(G;G)

Make rs1060499763(G;T)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

62140447

Gene

PIGN

is a	snp
is	mentioned by
dbSNP	rs1060499763
dbSNP (classic)	rs1060499763
ClinGen	rs1060499763
ebi	rs1060499763
HLI	rs1060499763
Exac	rs1060499763
Gnomad	rs1060499763
Varsome	rs1060499763
LitVar	rs1060499763
Map	rs1060499763
PheGenI	rs1060499763
Biobank	rs1060499763
1000 genomes	rs1060499763
hgdp	rs1060499763
ensembl	rs1060499763
geneview	rs1060499763
scholar	rs1060499763
google	rs1060499763
pharmgkb	rs1060499763
gwascentral	rs1060499763
openSNP	rs1060499763
23andMe	rs1060499763
SNPshot	rs1060499763
SNPdbe	rs1060499763
MSV3d	rs1060499763
GWAS Ctlg	rs1060499763

Max Magnitude

0

ClinVar
Risk	rs1060499763(G;G)
Alt	rs1060499763(G;G)
Reference	Rs1060499763(T;T)
Significance	Probable-Pathogenic
Disease	Abnormality of brain morphology
Variation	info
Gene	PIGN
CLNDBN	Abnormality of brain morphology
Reversed	1
HGVS	NC_000018.9:g.59807680A>C
CLNSRC
CLNACC	RCV000454324.1,