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rs397514262

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397514262(A;A)
Make rs397514262(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position211424241
GeneERBB4
is asnp
is mentioned by
dbSNPrs397514262
ebirs397514262
HLIrs397514262
Exacrs397514262
Varsomers397514262
Maprs397514262
PheGenIrs397514262
hapmaprs397514262
1000 genomesrs397514262
hgdprs397514262
ensemblrs397514262
gopubmedrs397514262
geneviewrs397514262
scholarrs397514262
googlers397514262
pharmgkbrs397514262
gwascentralrs397514262
openSNPrs397514262
23andMers397514262
23andMe allrs397514262
SNP Nexus

SNPshotrs397514262
SNPdbers397514262
MSV3drs397514262
GWAS Ctlgrs397514262
Max Magnitude0
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
CLNACC RCV000054812.1, RCV000074382.4,