rs121909535

Orientation

plus

Stabilized

plus

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

Make rs121909535(A;T)

Make rs121909535(T;T)

Reference

GRCh38 38.1/141

Chromosome

14

Position

20693671

Gene	ANG, RNASE4

is a	snp
is	mentioned by
dbSNP	rs121909535
dbSNP (classic)	rs121909535
ClinGen	rs121909535
ebi	rs121909535
HLI	rs121909535
Exac	rs121909535
Gnomad	rs121909535
Varsome	rs121909535
LitVar	rs121909535
Map	rs121909535
PheGenI	rs121909535
Biobank	rs121909535
1000 genomes	rs121909535
hgdp	rs121909535
ensembl	rs121909535
geneview	rs121909535
scholar	rs121909535
google	rs121909535
pharmgkb	rs121909535
gwascentral	rs121909535
openSNP	rs121909535
23andMe	rs121909535
SNPshot	rs121909535
SNPdbe	rs121909535
MSV3d	rs121909535
GWAS Ctlg	rs121909535

Max Magnitude

0

OMIM	105850
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121909535(T;T)
Alt	rs121909535(T;T)
Reference	Rs121909535(A;A)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 9
Variation	info
Gene	RNASE4 ANG
CLNDBN	Amyotrophic lateral sclerosis type 9
Reversed	0
HGVS	NC_000014.8:g.21161830A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019699.27,