rs797044934

Orientation

minus

Stabilized

minus

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

Make rs797044934(C;T)

Make rs797044934(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

201704160

Gene

ALS2

is a	snp
is	mentioned by
dbSNP	rs797044934
dbSNP (classic)	rs797044934
ClinGen	rs797044934
ebi	rs797044934
HLI	rs797044934
Exac	rs797044934
Gnomad	rs797044934
Varsome	rs797044934
LitVar	rs797044934
Map	rs797044934
PheGenI	rs797044934
Biobank	rs797044934
1000 genomes	rs797044934
hgdp	rs797044934
ensembl	rs797044934
geneview	rs797044934
scholar	rs797044934
google	rs797044934
pharmgkb	rs797044934
gwascentral	rs797044934
openSNP	rs797044934
23andMe	rs797044934
SNPshot	rs797044934
SNPdbe	rs797044934
MSV3d	rs797044934
GWAS Ctlg	rs797044934

Max Magnitude

0

ClinVar
Risk	rs797044934(T;T)
Alt	rs797044934(T;T)
Reference	Rs797044934(C;C)
Significance	Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	ALS2
CLNDBN	Inborn genetic diseases
Reversed	1
HGVS	NC_000002.11:g.202568883G>A
CLNSRC
CLNACC	RCV000190777.1,