rs3219156

Orientation

minus

Stabilized

minus

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

Make rs3219156(A;A)

Make rs3219156(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

201760892

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs3219156
dbSNP (classic)	rs3219156
ClinGen	rs3219156
ebi	rs3219156
HLI	rs3219156
Exac	rs3219156
Gnomad	rs3219156
Varsome	rs3219156
LitVar	rs3219156
Map	rs3219156
PheGenI	rs3219156
Biobank	rs3219156
1000 genomes	rs3219156
hgdp	rs3219156
ensembl	rs3219156
geneview	rs3219156
scholar	rs3219156
google	rs3219156
pharmgkb	rs3219156
gwascentral	rs3219156
openSNP	rs3219156
23andMe	rs3219156
SNPshot	rs3219156
SNPdbe	rs3219156
MSV3d	rs3219156
GWAS Ctlg	rs3219156

GMAF

0.101

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs3219156(A;A)
Alt	rs3219156(A;A)
Reference	Rs3219156(G;G)
Significance	Non-pathogenic
Disease	not specified ALS2-Related Spectrum Disorders Amyotrophic Lateral Sclerosis
Variation	info
Gene	ALS2
CLNDBN	not specified ALS2-Related Spectrum Disorders Amyotrophic Lateral Sclerosis, Recessive
Reversed	1
HGVS	NC_000002.11:g.202625615C>T
CLNSRC
CLNACC	RCV000243956.1, RCV000269440.1, RCV000326864.1,