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rs1060499761

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499761(G;G)
Make rs1060499761(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position87934803
GeneGALC
is asnp
is mentioned by
dbSNPrs1060499761
dbSNP (old)rs1060499761
ClinGenrs1060499761
ebirs1060499761
HLIrs1060499761
Exacrs1060499761
Gnomadrs1060499761
Varsomers1060499761
Maprs1060499761
PheGenIrs1060499761
Biobankrs1060499761
1000 genomesrs1060499761
hgdprs1060499761
ensemblrs1060499761
gopubmedrs1060499761
geneviewrs1060499761
scholarrs1060499761
googlers1060499761
pharmgkbrs1060499761
gwascentralrs1060499761
openSNPrs1060499761
23andMers1060499761
23andMe allrs1060499761
SNPshotrs1060499761
SNPdbers1060499761
MSV3drs1060499761
GWAS Ctlgrs1060499761
Max Magnitude0
ClinVar
Risk rs1060499761(G;G)
Alt rs1060499761(G;G)
Reference Rs1060499761(T;T)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene GALC
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000014.8:g.88401147A>C
CLNSRC
CLNACC RCV000454130.1,