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rs587777071

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777071(A;A)
Make rs587777071(A;G)
ReferenceGRCh38 38.1/142
Chromosome13
Position85795968
GeneSLITRK6
is asnp
is mentioned by
dbSNPrs587777071
ebirs587777071
HLIrs587777071
Exacrs587777071
Varsomers587777071
Maprs587777071
PheGenIrs587777071
hapmaprs587777071
1000 genomesrs587777071
hgdprs587777071
ensemblrs587777071
gopubmedrs587777071
geneviewrs587777071
scholarrs587777071
googlers587777071
pharmgkbrs587777071
gwascentralrs587777071
openSNPrs587777071
23andMers587777071
23andMe allrs587777071
SNP Nexus

SNPshotrs587777071
SNPdbers587777071
MSV3drs587777071
GWAS Ctlgrs587777071
Max Magnitude0
ClinVar
Risk rs587777071(A;A)
Alt rs587777071(A;A)
Reference rs587777071(G;G)
Significance Pathogenic
Disease Deafness and myopia
Variation info
Gene SLITRK6
CLNDBN Deafness and myopia
Reversed 0
HGVS NC_000013.10:g.86370103G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000074450.3,