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rs587777072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs587777072(-;-)
Make rs587777072(-;AT)
ReferenceGRCh38 38.1/142
Chromosome19
Position36008267
GeneSYNE4
is asnp
is mentioned by
dbSNPrs587777072
ebirs587777072
HLIrs587777072
Exacrs587777072
Varsomers587777072
Maprs587777072
PheGenIrs587777072
hapmaprs587777072
1000 genomesrs587777072
hgdprs587777072
ensemblrs587777072
gopubmedrs587777072
geneviewrs587777072
scholarrs587777072
googlers587777072
pharmgkbrs587777072
gwascentralrs587777072
openSNPrs587777072
23andMers587777072
23andMe allrs587777072
SNP Nexus

SNPshotrs587777072
SNPdbers587777072
MSV3drs587777072
GWAS Ctlgrs587777072
Max Magnitude0
ClinVar
Risk rs587777072(;)
Alt rs587777072(;)
Reference rs587777072(AT;AT)
Significance Pathogenic
Disease Deafness
Variation info
Gene SYNE4
CLNDBN Deafness, autosomal recessive 76
Reversed 1
HGVS NC_000019.9:g.36499169_36499170delAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000074459.4,