rs121909536

Orientation

plus

Stabilized

plus

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

Make rs121909536(A;T)

Make rs121909536(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

20693686

Gene	ANG, RNASE4

is a	snp
is	mentioned by
dbSNP	rs121909536
dbSNP (classic)	rs121909536
ClinGen	rs121909536
ebi	rs121909536
HLI	rs121909536
Exac	rs121909536
Gnomad	rs121909536
Varsome	rs121909536
LitVar	rs121909536
Map	rs121909536
PheGenI	rs121909536
Biobank	rs121909536
1000 genomes	rs121909536
hgdp	rs121909536
ensembl	rs121909536
geneview	rs121909536
scholar	rs121909536
google	rs121909536
pharmgkb	rs121909536
gwascentral	rs121909536
openSNP	rs121909536
23andMe	rs121909536
SNPshot	rs121909536
SNPdbe	rs121909536
MSV3d	rs121909536
GWAS Ctlg	rs121909536

GMAF

0.0004591

Max Magnitude

0

OMIM	105850
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909536(T;T)
Alt	rs121909536(T;T)
Reference	Rs121909536(A;A)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 9 Amyotrophic Lateral Sclerosis
Variation	info
Gene	RNASE4 ANG
CLNDBN	Amyotrophic lateral sclerosis type 9 Amyotrophic Lateral Sclerosis, Dominant
Reversed	0
HGVS	NC_000014.8:g.21161845A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019700.27, RCV000374265.1,