rs398124396

Orientation

minus

Stabilized

minus

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

Make rs398124396(-;-)

Make rs398124396(-;AT)

Reference

GRCh38 38.1/141

Chromosome

12

Position

101770482

Gene

GNPTAB

is a	snp
is	mentioned by
dbSNP	rs398124396
dbSNP (classic)	rs398124396
ClinGen	rs398124396
ebi	rs398124396
HLI	rs398124396
Exac	rs398124396
Gnomad	rs398124396
Varsome	rs398124396
LitVar	rs398124396
Map	rs398124396
PheGenI	rs398124396
Biobank	rs398124396
1000 genomes	rs398124396
hgdp	rs398124396
ensembl	rs398124396
geneview	rs398124396
scholar	rs398124396
google	rs398124396
pharmgkb	rs398124396
gwascentral	rs398124396
openSNP	rs398124396
23andMe	rs398124396
SNPshot	rs398124396
SNPdbe	rs398124396
MSV3d	rs398124396
GWAS Ctlg	rs398124396

Max Magnitude

0

ClinVar
Risk	rs398124396(-;-)
Alt	rs398124396(-;-)
Reference	Rs398124396(AT;AT)
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.102164260_102164261delAT
CLNSRC	ClinVar
CLNACC	RCV000082185.3, RCV000180685.1,