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rs1060499746

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060499746(A;A)
Make rs1060499746(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position27481179
GeneGTF3C1
is asnp
is mentioned by
dbSNPrs1060499746
dbSNP (old)rs1060499746
ClinGenrs1060499746
ebirs1060499746
HLIrs1060499746
Exacrs1060499746
Gnomadrs1060499746
Varsomers1060499746
Maprs1060499746
PheGenIrs1060499746
Biobankrs1060499746
1000 genomesrs1060499746
hgdprs1060499746
ensemblrs1060499746
gopubmedrs1060499746
geneviewrs1060499746
scholarrs1060499746
googlers1060499746
pharmgkbrs1060499746
gwascentralrs1060499746
openSNPrs1060499746
23andMers1060499746
23andMe allrs1060499746
SNPshotrs1060499746
SNPdbers1060499746
MSV3drs1060499746
GWAS Ctlgrs1060499746
Max Magnitude0
ClinVar
Risk rs1060499746(A;A)
Alt rs1060499746(A;A)
Reference Rs1060499746(G;G)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene GTF3C1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000016.9:g.27492500C>T
CLNSRC
CLNACC RCV000454278.1,