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rs1060499755

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1060499755(A;G)
Make rs1060499755(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position126577158
GeneALDH7A1
is asnp
is mentioned by
dbSNPrs1060499755
dbSNP (old)rs1060499755
ClinGenrs1060499755
ebirs1060499755
HLIrs1060499755
Exacrs1060499755
Gnomadrs1060499755
Varsomers1060499755
Maprs1060499755
PheGenIrs1060499755
Biobankrs1060499755
1000 genomesrs1060499755
hgdprs1060499755
ensemblrs1060499755
gopubmedrs1060499755
geneviewrs1060499755
scholarrs1060499755
googlers1060499755
pharmgkbrs1060499755
gwascentralrs1060499755
openSNPrs1060499755
23andMers1060499755
23andMe allrs1060499755
SNPshotrs1060499755
SNPdbers1060499755
MSV3drs1060499755
GWAS Ctlgrs1060499755
Max Magnitude0
ClinVar
Risk rs1060499755(G;G)
Alt rs1060499755(G;G)
Reference Rs1060499755(A;A)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene ALDH7A1
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000005.9:g.125912850T>C
CLNSRC
CLNACC RCV000454207.1,