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rs587777069

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777069(A;A)
Make rs587777069(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position85795269
GeneSLITRK6
is asnp
is mentioned by
dbSNPrs587777069
ebirs587777069
HLIrs587777069
Exacrs587777069
Varsomers587777069
Maprs587777069
PheGenIrs587777069
hapmaprs587777069
1000 genomesrs587777069
hgdprs587777069
ensemblrs587777069
gopubmedrs587777069
geneviewrs587777069
scholarrs587777069
googlers587777069
pharmgkbrs587777069
gwascentralrs587777069
openSNPrs587777069
23andMers587777069
23andMe allrs587777069
SNP Nexus

SNPshotrs587777069
SNPdbers587777069
MSV3drs587777069
GWAS Ctlgrs587777069
Max Magnitude0
ClinVar
Risk rs587777069(A;A)
Alt rs587777069(A;A)
Reference rs587777069(G;G)
Significance Pathogenic
Disease Deafness and myopia
Variation info
Gene SLITRK6
CLNDBN Deafness and myopia
Reversed 0
HGVS NC_000013.10:g.86369404G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074448.6,