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rs1060499751

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060499751(C;T)
Make rs1060499751(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position153659157
GeneSNAPIN
is asnp
is mentioned by
dbSNPrs1060499751
dbSNP (old)rs1060499751
ClinGenrs1060499751
ebirs1060499751
HLIrs1060499751
Exacrs1060499751
Gnomadrs1060499751
Varsomers1060499751
Maprs1060499751
PheGenIrs1060499751
Biobankrs1060499751
1000 genomesrs1060499751
hgdprs1060499751
ensemblrs1060499751
gopubmedrs1060499751
geneviewrs1060499751
scholarrs1060499751
googlers1060499751
pharmgkbrs1060499751
gwascentralrs1060499751
openSNPrs1060499751
23andMers1060499751
23andMe allrs1060499751
SNPshotrs1060499751
SNPdbers1060499751
MSV3drs1060499751
GWAS Ctlgrs1060499751
Max Magnitude0
ClinVar
Risk rs1060499751(T;T)
Alt rs1060499751(T;T)
Reference Rs1060499751(C;C)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene SNAPIN
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000001.10:g.153631633C>T
CLNSRC
CLNACC RCV000454257.1,