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rs1060499750

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499750(C;C)
Make rs1060499750(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome13
Position87677903
GeneSLITRK5
is asnp
is mentioned by
dbSNPrs1060499750
dbSNP (old)rs1060499750
ClinGenrs1060499750
ebirs1060499750
HLIrs1060499750
Exacrs1060499750
Gnomadrs1060499750
Varsomers1060499750
Maprs1060499750
PheGenIrs1060499750
Biobankrs1060499750
1000 genomesrs1060499750
hgdprs1060499750
ensemblrs1060499750
gopubmedrs1060499750
geneviewrs1060499750
scholarrs1060499750
googlers1060499750
pharmgkbrs1060499750
gwascentralrs1060499750
openSNPrs1060499750
23andMers1060499750
23andMe allrs1060499750
SNPshotrs1060499750
SNPdbers1060499750
MSV3drs1060499750
GWAS Ctlgrs1060499750
Max Magnitude0
ClinVar
Risk rs1060499750(C;C)
Alt rs1060499750(C;C)
Reference Rs1060499750(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene SLITRK5
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000013.10:g.88330158G>C
CLNSRC
CLNACC RCV000454171.1,