rs267606929

Orientation

plus

Stabilized

plus

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

Make rs267606929(A;G)

Make rs267606929(G;G)

Reference

GRCh38 38.1/141

Chromosome

10

Position

13132098

Gene

OPTN

is a	snp
is	mentioned by
dbSNP	rs267606929
dbSNP (classic)	rs267606929
ClinGen	rs267606929
ebi	rs267606929
HLI	rs267606929
Exac	rs267606929
Gnomad	rs267606929
Varsome	rs267606929
LitVar	rs267606929
Map	rs267606929
PheGenI	rs267606929
Biobank	rs267606929
1000 genomes	rs267606929
hgdp	rs267606929
ensembl	rs267606929
geneview	rs267606929
scholar	rs267606929
google	rs267606929
pharmgkb	rs267606929
gwascentral	rs267606929
openSNP	rs267606929
23andMe	rs267606929
SNPshot	rs267606929
SNPdbe	rs267606929
MSV3d	rs267606929
GWAS Ctlg	rs267606929

Max Magnitude

0

ClinVar
Risk	rs267606929(G;G)
Alt	rs267606929(G;G)
Reference	Rs267606929(A;A)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 12
Variation	info
Gene	OPTN
CLNDBN	Amyotrophic lateral sclerosis type 12
Reversed	0
HGVS	NC_000010.10:g.13174098A>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000007520.3,