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rs398124619

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398124619(G;T)
Make rs398124619(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position215970720
GeneUSH2A
is asnp
is mentioned by
dbSNPrs398124619
ebirs398124619
HLIrs398124619
Exacrs398124619
Varsomers398124619
Maprs398124619
PheGenIrs398124619
hapmaprs398124619
1000 genomesrs398124619
hgdprs398124619
ensemblrs398124619
gopubmedrs398124619
geneviewrs398124619
scholarrs398124619
googlers398124619
pharmgkbrs398124619
gwascentralrs398124619
openSNPrs398124619
23andMers398124619
23andMe allrs398124619
SNP Nexus

SNPshotrs398124619
SNPdbers398124619
MSV3drs398124619
GWAS Ctlgrs398124619
Max Magnitude0
ClinVar
Risk rs398124619(T;T)
Alt rs398124619(T;T)
Reference rs398124619(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.216144062C>A
CLNSRC HGMD
CLNACC RCV000082830.4,