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rs786205880

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs786205880(-;-)
Make rs786205880(-;TC)
Make rs786205880(TC;TC)
ReferenceGRCh38.p2 38.2/146
Chromosome20
Position62260099
GeneOSBPL2
is asnp
is mentioned by
dbSNPrs786205880
ebirs786205880
HLIrs786205880
Exacrs786205880
Varsomers786205880
Maprs786205880
PheGenIrs786205880
hapmaprs786205880
1000 genomesrs786205880
hgdprs786205880
ensemblrs786205880
gopubmedrs786205880
geneviewrs786205880
scholarrs786205880
googlers786205880
pharmgkbrs786205880
gwascentralrs786205880
openSNPrs786205880
23andMers786205880
23andMe allrs786205880
SNP Nexus

SNPshotrs786205880
SNPdbers786205880
MSV3drs786205880
GWAS Ctlgrs786205880
Max Magnitude0
ClinVar
Risk rs786205880(;)
Alt rs786205880(;)
Reference rs786205880(CT;CT)
Significance Pathogenic
Disease Deafness
Variation info
Gene OSBPL2
CLNDBN Deafness, autosomal dominant 67
Reversed 0
HGVS NC_000020.10:g.60835155_60835156delTC
CLNSRC OMIM Allelic Variant
CLNACC RCV000170349.3,