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rs398124618

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GA;GA) 0 common in clinvar
Make rs398124618(-;-)
Make rs398124618(-;GA)
ReferenceGRCh38 38.1/141
Chromosome1
Position215680208
GeneUSH2A
is asnp
is mentioned by
dbSNPrs398124618
ebirs398124618
HLIrs398124618
Exacrs398124618
Varsomers398124618
Maprs398124618
PheGenIrs398124618
hapmaprs398124618
1000 genomesrs398124618
hgdprs398124618
ensemblrs398124618
gopubmedrs398124618
geneviewrs398124618
scholarrs398124618
googlers398124618
pharmgkbrs398124618
gwascentralrs398124618
openSNPrs398124618
23andMers398124618
23andMe allrs398124618
SNP Nexus

SNPshotrs398124618
SNPdbers398124618
MSV3drs398124618
GWAS Ctlgrs398124618
Max Magnitude0
ClinVar
Risk rs398124618(;)
Alt rs398124618(;)
Reference rs398124618(GA;GA)
Significance Pathogenic
Disease not provided
Variation info
Gene USH2A
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.215853550_215853551delTC
CLNSRC HGMD
CLNACC RCV000082828.4,