rs587777912

Merged into

rs281865032

Orientation

minus

Stabilized

minus

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

Make rs587777912(-;T)

Make rs587777912(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

12

Position

101761344

Gene

GNPTAB

is a	snp
is	mentioned by
dbSNP	rs587777912
dbSNP (classic)	rs587777912
ClinGen	rs587777912
ebi	rs587777912
HLI	rs587777912
Exac	rs587777912
Gnomad	rs587777912
Varsome	rs587777912
LitVar	rs587777912
Map	rs587777912
PheGenI	rs587777912
Biobank	rs587777912
1000 genomes	rs587777912
hgdp	rs587777912
ensembl	rs587777912
geneview	rs587777912
scholar	rs587777912
google	rs587777912
pharmgkb	rs587777912
gwascentral	rs587777912
openSNP	rs587777912
23andMe	rs587777912
SNPshot	rs587777912
SNPdbe	rs587777912
MSV3d	rs587777912
GWAS Ctlg	rs587777912

Status

Merged into rs281865032

Max Magnitude

0

ClinVar
Risk	rs587777912(T;T)
Alt	rs587777912(T;T)
Reference	Rs587777912(;)
Significance	Pathogenic
Disease	I cell disease
Variation	info
Gene	GNPTAB
CLNDBN	I cell disease
Reversed	1
HGVS	NC_000012.11:g.102155123dupA
CLNSRC
CLNACC	RCV000031977.2,