rs1060499666

Orientation

minus

Stabilized

minus

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

Make rs1060499666(A;A)

Make rs1060499666(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

X

Position

15324670

Gene

PIGA

is a	snp
is	mentioned by
dbSNP	rs1060499666
dbSNP (classic)	rs1060499666
ClinGen	rs1060499666
ebi	rs1060499666
HLI	rs1060499666
Exac	rs1060499666
Gnomad	rs1060499666
Varsome	rs1060499666
LitVar	rs1060499666
Map	rs1060499666
PheGenI	rs1060499666
Biobank	rs1060499666
1000 genomes	rs1060499666
hgdp	rs1060499666
ensembl	rs1060499666
geneview	rs1060499666
scholar	rs1060499666
google	rs1060499666
pharmgkb	rs1060499666
gwascentral	rs1060499666
openSNP	rs1060499666
23andMe	rs1060499666
SNPshot	rs1060499666
SNPdbe	rs1060499666
MSV3d	rs1060499666
GWAS Ctlg	rs1060499666

Max Magnitude

0

ClinVar
Risk	rs1060499666(A;A)
Alt	rs1060499666(A;A)
Reference	Rs1060499666(G;G)
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.15342792C>T
CLNSRC
CLNACC	RCV000449490.1,