rs200199765

Orientation

plus

Stabilized

plus

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

Make rs200199765(A;A)

Make rs200199765(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

62161173

Gene

PIGN

is a	snp
is	mentioned by
dbSNP	rs200199765
dbSNP (classic)	rs200199765
ClinGen	rs200199765
ebi	rs200199765
HLI	rs200199765
Exac	rs200199765
Gnomad	rs200199765
Varsome	rs200199765
LitVar	rs200199765
Map	rs200199765
PheGenI	rs200199765
Biobank	rs200199765
1000 genomes	rs200199765
hgdp	rs200199765
ensembl	rs200199765
geneview	rs200199765
scholar	rs200199765
google	rs200199765
pharmgkb	rs200199765
gwascentral	rs200199765
openSNP	rs200199765
23andMe	rs200199765
SNPshot	rs200199765
SNPdbe	rs200199765
MSV3d	rs200199765
GWAS Ctlg	rs200199765

Max Magnitude

0

ClinVar
Risk	rs200199765(A;A)
Alt	rs200199765(A;A)
Reference	Rs200199765(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	PIGN
CLNDBN	not provided
Reversed	0
HGVS	NC_000018.9:g.59828406C>A
CLNSRC
CLNACC	RCV000412737.1,