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rs1060499741

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499741(-;-)
Make rs1060499741(-;C)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position117255281
GeneSLC18A2
is asnp
is mentioned by
dbSNPrs1060499741
dbSNP (old)rs1060499741
ClinGenrs1060499741
ebirs1060499741
HLIrs1060499741
Exacrs1060499741
Gnomadrs1060499741
Varsomers1060499741
LitVarrs1060499741
Maprs1060499741
PheGenIrs1060499741
Biobankrs1060499741
1000 genomesrs1060499741
hgdprs1060499741
ensemblrs1060499741
gopubmedrs1060499741
geneviewrs1060499741
scholarrs1060499741
googlers1060499741
pharmgkbrs1060499741
gwascentralrs1060499741
openSNPrs1060499741
23andMers1060499741
23andMe allrs1060499741
SNPshotrs1060499741
SNPdbers1060499741
MSV3drs1060499741
GWAS Ctlgrs1060499741
Max Magnitude0
ClinVar
Risk rs1060499741(-;-)
Alt rs1060499741(-;-)
Reference Rs1060499741(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene SLC18A2
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000010.10:g.119014792delC
CLNSRC
CLNACC RCV000454269.1,