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rs1060499754

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499754(A;G)
Make rs1060499754(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position19797472
GeneULK2
is asnp
is mentioned by
dbSNPrs1060499754
dbSNP (old)rs1060499754
ClinGenrs1060499754
ebirs1060499754
HLIrs1060499754
Exacrs1060499754
Gnomadrs1060499754
Varsomers1060499754
Maprs1060499754
PheGenIrs1060499754
Biobankrs1060499754
1000 genomesrs1060499754
hgdprs1060499754
ensemblrs1060499754
gopubmedrs1060499754
geneviewrs1060499754
scholarrs1060499754
googlers1060499754
pharmgkbrs1060499754
gwascentralrs1060499754
openSNPrs1060499754
23andMers1060499754
23andMe allrs1060499754
SNPshotrs1060499754
SNPdbers1060499754
MSV3drs1060499754
GWAS Ctlgrs1060499754
Max Magnitude0
ClinVar
Risk rs1060499754(G;G)
Alt rs1060499754(G;G)
Reference Rs1060499754(A;A)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene ULK2
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000017.10:g.19700785T>C
CLNSRC
CLNACC RCV000454305.1,