rs767350733

Orientation

plus

Stabilized

plus

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

Make rs767350733(A;A)

Make rs767350733(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

201724392

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs767350733
dbSNP (classic)	rs767350733
ClinGen	rs767350733
ebi	rs767350733
HLI	rs767350733
Exac	rs767350733
Gnomad	rs767350733
Varsome	rs767350733
LitVar	rs767350733
Map	rs767350733
PheGenI	rs767350733
Biobank	rs767350733
1000 genomes	rs767350733
hgdp	rs767350733
ensembl	rs767350733
geneview	rs767350733
scholar	rs767350733
google	rs767350733
pharmgkb	rs767350733
gwascentral	rs767350733
openSNP	rs767350733
23andMe	rs767350733
SNPshot	rs767350733
SNPdbe	rs767350733
MSV3d	rs767350733
GWAS Ctlg	rs767350733

Max Magnitude

0

ClinVar
Risk	rs767350733(A;A)
Alt	rs767350733(A;A)
Reference	Rs767350733(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ALS2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.202589115G>A
CLNSRC
CLNACC	RCV000421128.1,