rs398124398

Orientation

minus

Stabilized

minus

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

Make rs398124398(-;-)

Make rs398124398(-;A)

Reference

GRCh38 38.1/141

Chromosome

12

Position

101761583

Gene

GNPTAB

is a	snp
is	mentioned by
dbSNP	rs398124398
dbSNP (classic)	rs398124398
ClinGen	rs398124398
ebi	rs398124398
HLI	rs398124398
Exac	rs398124398
Gnomad	rs398124398
Varsome	rs398124398
LitVar	rs398124398
Map	rs398124398
PheGenI	rs398124398
Biobank	rs398124398
1000 genomes	rs398124398
hgdp	rs398124398
ensembl	rs398124398
geneview	rs398124398
scholar	rs398124398
google	rs398124398
pharmgkb	rs398124398
gwascentral	rs398124398
openSNP	rs398124398
23andMe	rs398124398
SNPshot	rs398124398
SNPdbe	rs398124398
MSV3d	rs398124398
GWAS Ctlg	rs398124398

Max Magnitude

0

ClinVar
Risk	rs398124398(-;-)
Alt	rs398124398(-;-)
Reference	Rs398124398(A;A)
Significance	Pathogenic
Disease	not provided I cell disease
Variation	info
Gene	GNPTAB
CLNDBN	not provided I cell disease
Reversed	1
HGVS	NC_000012.11:g.102155361delT
CLNSRC	ClinVar
CLNACC	RCV000082190.3, RCV000174796.1,