rs1060499625

Orientation

minus

Stabilized

minus

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

Make rs1060499625(C;G)

Make rs1060499625(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

15331536

Gene

PIGA

is a	snp
is	mentioned by
dbSNP	rs1060499625
dbSNP (classic)	rs1060499625
ClinGen	rs1060499625
ebi	rs1060499625
HLI	rs1060499625
Exac	rs1060499625
Gnomad	rs1060499625
Varsome	rs1060499625
LitVar	rs1060499625
Map	rs1060499625
PheGenI	rs1060499625
Biobank	rs1060499625
1000 genomes	rs1060499625
hgdp	rs1060499625
ensembl	rs1060499625
geneview	rs1060499625
scholar	rs1060499625
google	rs1060499625
pharmgkb	rs1060499625
gwascentral	rs1060499625
openSNP	rs1060499625
23andMe	rs1060499625
SNPshot	rs1060499625
SNPdbe	rs1060499625
MSV3d	rs1060499625
GWAS Ctlg	rs1060499625

Max Magnitude

0

ClinVar
Risk	rs1060499625(G;G)
Alt	rs1060499625(G;G)
Reference	Rs1060499625(C;C)
Significance	Probable-Pathogenic
Disease	Multiple congenital anomalies-hypotonia-seizures syndrome 2
Variation	info
Gene	PIGA
CLNDBN	Multiple congenital anomalies-hypotonia-seizures syndrome 2
Reversed	1
HGVS	NC_000023.10:g.15349658G>C
CLNSRC
CLNACC	RCV000445622.1,