rs761291489

Orientation

plus

Stabilized

plus

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

Make rs761291489(C;T)

Make rs761291489(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

201711091

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs761291489
dbSNP (classic)	rs761291489
ClinGen	rs761291489
ebi	rs761291489
HLI	rs761291489
Exac	rs761291489
Gnomad	rs761291489
Varsome	rs761291489
LitVar	rs761291489
Map	rs761291489
PheGenI	rs761291489
Biobank	rs761291489
1000 genomes	rs761291489
hgdp	rs761291489
ensembl	rs761291489
geneview	rs761291489
scholar	rs761291489
google	rs761291489
pharmgkb	rs761291489
gwascentral	rs761291489
openSNP	rs761291489
23andMe	rs761291489
SNPshot	rs761291489
SNPdbe	rs761291489
MSV3d	rs761291489
GWAS Ctlg	rs761291489

Max Magnitude

0

ClinVar
Risk	rs761291489(T;T)
Alt	rs761291489(T;T)
Reference	Rs761291489(C;C)
Significance	Probable-Pathogenic
Disease	Peripheral axonal neuropathy
Variation	info
Gene	ALS2
CLNDBN	Peripheral axonal neuropathy
Reversed	0
HGVS	NC_000002.11:g.202575814C>T
CLNSRC
CLNACC	RCV000415216.1,