rs72466496

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs72466496(C;T)

Make rs72466496(T;T)

Reference

GRCh38 38.1/142

Chromosome

2

Position

74361590

Gene

DCTN1

is a	snp
is	mentioned by
dbSNP	rs72466496
dbSNP (classic)	rs72466496
ClinGen	rs72466496
ebi	rs72466496
HLI	rs72466496
Exac	rs72466496
Gnomad	rs72466496
Varsome	rs72466496
LitVar	rs72466496
Map	rs72466496
PheGenI	rs72466496
Biobank	rs72466496
1000 genomes	rs72466496
hgdp	rs72466496
ensembl	rs72466496
geneview	rs72466496
scholar	rs72466496
google	rs72466496
pharmgkb	rs72466496
gwascentral	rs72466496
openSNP	rs72466496
23andMe	rs72466496
SNPshot	rs72466496
SNPdbe	rs72466496
MSV3d	rs72466496
GWAS Ctlg	rs72466496

GMAF

0.0004591

Max Magnitude

0

OMIM	601143
Desc
Variant	0002
Related	also

ClinVar
Risk	rs72466496(T;T)
Alt	rs72466496(T;T)
Reference	Rs72466496(C;C)
Significance	Other
Disease	Amyotrophic lateral sclerosis not provided Perry syndrome
Variation	info
Gene	DCTN1
CLNDBN	Amyotrophic lateral sclerosis, susceptibility to not provided Perry syndrome
Reversed	1
HGVS	NC_000002.11:g.74588717G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008910.2, RCV000143802.1, RCV000263003.1,