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rs786205881

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs786205881(-;-)
Make rs786205881(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome20
Position62260084
GeneOSBPL2
is asnp
is mentioned by
dbSNPrs786205881
ebirs786205881
HLIrs786205881
Exacrs786205881
Varsomers786205881
Maprs786205881
PheGenIrs786205881
hapmaprs786205881
1000 genomesrs786205881
hgdprs786205881
ensemblrs786205881
gopubmedrs786205881
geneviewrs786205881
scholarrs786205881
googlers786205881
pharmgkbrs786205881
gwascentralrs786205881
openSNPrs786205881
23andMers786205881
23andMe allrs786205881
SNP Nexus

SNPshotrs786205881
SNPdbers786205881
MSV3drs786205881
GWAS Ctlgrs786205881
Max Magnitude0
ClinVar
Risk rs786205881(;)
Alt rs786205881(;)
Reference rs786205881(TG;TG)
Significance Pathogenic
Disease Deafness
Variation info
Gene OSBPL2
CLNDBN Deafness, autosomal dominant 67
Reversed 0
HGVS NC_000020.10:g.60835140_60835141delTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000170350.3,