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rs1060499742

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499742(C;T)
Make rs1060499742(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position60071229
GeneANK3
is asnp
is mentioned by
dbSNPrs1060499742
dbSNP (old)rs1060499742
ClinGenrs1060499742
ebirs1060499742
HLIrs1060499742
Exacrs1060499742
Gnomadrs1060499742
Varsomers1060499742
Maprs1060499742
PheGenIrs1060499742
Biobankrs1060499742
1000 genomesrs1060499742
hgdprs1060499742
ensemblrs1060499742
gopubmedrs1060499742
geneviewrs1060499742
scholarrs1060499742
googlers1060499742
pharmgkbrs1060499742
gwascentralrs1060499742
openSNPrs1060499742
23andMers1060499742
23andMe allrs1060499742
SNPshotrs1060499742
SNPdbers1060499742
MSV3drs1060499742
GWAS Ctlgrs1060499742
Max Magnitude0
ClinVar
Risk rs1060499742(T;T)
Alt rs1060499742(T;T)
Reference Rs1060499742(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene ANK3
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000010.10:g.61830987G>A
CLNSRC
CLNACC RCV000454308.1,