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rs587777070

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777070(G;T)
Make rs587777070(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position85795619
GeneSLITRK6
is asnp
is mentioned by
dbSNPrs587777070
ebirs587777070
HLIrs587777070
Exacrs587777070
Varsomers587777070
Maprs587777070
PheGenIrs587777070
hapmaprs587777070
1000 genomesrs587777070
hgdprs587777070
ensemblrs587777070
gopubmedrs587777070
geneviewrs587777070
scholarrs587777070
googlers587777070
pharmgkbrs587777070
gwascentralrs587777070
openSNPrs587777070
23andMers587777070
23andMe allrs587777070
SNP Nexus

SNPshotrs587777070
SNPdbers587777070
MSV3drs587777070
GWAS Ctlgrs587777070
Max Magnitude0
ClinVar
Risk rs587777070(G,T;G,T)
Alt rs587777070(G,T;G,T)
Reference rs587777070(C;C)
Significance Pathogenic
Disease Deafness and myopia
Variation info
Gene SLITRK6
CLNDBN Deafness and myopia
Reversed 1
HGVS NC_000013.10:g.86369754G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074449.3,