rs397514262

Orientation

minus

Stabilized

minus

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

Make rs397514262(A;A)

Make rs397514262(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

211424241

Gene

ERBB4

is a	snp
is	mentioned by
dbSNP	rs397514262
dbSNP (classic)	rs397514262
ClinGen	rs397514262
ebi	rs397514262
HLI	rs397514262
Exac	rs397514262
Gnomad	rs397514262
Varsome	rs397514262
LitVar	rs397514262
Map	rs397514262
PheGenI	rs397514262
Biobank	rs397514262
1000 genomes	rs397514262
hgdp	rs397514262
ensembl	rs397514262
geneview	rs397514262
scholar	rs397514262
google	rs397514262
pharmgkb	rs397514262
gwascentral	rs397514262
openSNP	rs397514262
23andMe	rs397514262
SNPshot	rs397514262
SNPdbe	rs397514262
MSV3d	rs397514262
GWAS Ctlg	rs397514262

Max Magnitude

0

ClinVar
Risk	rs397514262(A;A)
Alt	rs397514262(A;A)
Reference	Rs397514262(G;G)
Significance	Pathogenic
Disease	not provided Amyotrophic lateral sclerosis 19
Variation	info
Gene	ERBB4
CLNDBN	not provided Amyotrophic lateral sclerosis 19
Reversed	1
HGVS	NC_000002.11:g.212288966C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000054812.1, RCV000074382.4,