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rs864309524

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864309524(C;C)
Make rs864309524(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome15
Position82854741
GeneHOMER2
is asnp
is mentioned by
dbSNPrs864309524
ebirs864309524
HLIrs864309524
Exacrs864309524
Varsomers864309524
Maprs864309524
PheGenIrs864309524
hapmaprs864309524
1000 genomesrs864309524
hgdprs864309524
ensemblrs864309524
gopubmedrs864309524
geneviewrs864309524
scholarrs864309524
googlers864309524
pharmgkbrs864309524
gwascentralrs864309524
openSNPrs864309524
23andMers864309524
23andMe allrs864309524
SNP Nexus

SNPshotrs864309524
SNPdbers864309524
MSV3drs864309524
GWAS Ctlgrs864309524
Max Magnitude0
ClinVar
Risk rs864309524(C;C)
Alt rs864309524(C;C)
Reference rs864309524(G;G)
Significance Pathogenic
Disease Deafness
Variation info
Gene HOMER2
CLNDBN Deafness, autosomal dominant 68
Reversed 1
HGVS NC_000015.9:g.83523493C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000202595.1,