rs121909541

Orientation

plus

Stabilized

plus

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

Make rs121909541(A;G)

Make rs121909541(G;G)

Reference

GRCh38 38.1/141

Chromosome

14

Position

20693772

Gene	ANG, RNASE4

is a	snp
is	mentioned by
dbSNP	rs121909541
dbSNP (classic)	rs121909541
ClinGen	rs121909541
ebi	rs121909541
HLI	rs121909541
Exac	rs121909541
Gnomad	rs121909541
Varsome	rs121909541
LitVar	rs121909541
Map	rs121909541
PheGenI	rs121909541
Biobank	rs121909541
1000 genomes	rs121909541
hgdp	rs121909541
ensembl	rs121909541
geneview	rs121909541
scholar	rs121909541
google	rs121909541
pharmgkb	rs121909541
gwascentral	rs121909541
openSNP	rs121909541
23andMe	rs121909541
SNPshot	rs121909541
SNPdbe	rs121909541
MSV3d	rs121909541
GWAS Ctlg	rs121909541

Max Magnitude

0

OMIM	105850
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909541(G;G)
Alt	rs121909541(G;G)
Reference	Rs121909541(A;A)
Significance	Pathogenic
Disease	Amyotrophic lateral sclerosis type 9 not specified
Variation	info
Gene	ANG RNASE4
CLNDBN	Amyotrophic lateral sclerosis type 9 not specified
Reversed	0
HGVS	NC_000014.8:g.21161931A>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019705.27, RCV000335176.1,