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rs1060499752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499752(G;G)
Make rs1060499752(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position160064970
GenePWWP2A, TTC1
is asnp
is mentioned by
dbSNPrs1060499752
dbSNP (old)rs1060499752
ClinGenrs1060499752
ebirs1060499752
HLIrs1060499752
Exacrs1060499752
Gnomadrs1060499752
Varsomers1060499752
LitVarrs1060499752
Maprs1060499752
PheGenIrs1060499752
Biobankrs1060499752
1000 genomesrs1060499752
hgdprs1060499752
ensemblrs1060499752
gopubmedrs1060499752
geneviewrs1060499752
scholarrs1060499752
googlers1060499752
pharmgkbrs1060499752
gwascentralrs1060499752
openSNPrs1060499752
23andMers1060499752
23andMe allrs1060499752
SNPshotrs1060499752
SNPdbers1060499752
MSV3drs1060499752
GWAS Ctlgrs1060499752
Max Magnitude0
ClinVar
Risk rs1060499752(G;G)
Alt rs1060499752(G;G)
Reference Rs1060499752(T;T)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene TTC1
CLNDBN Abnormality of brain morphology
Reversed 0
HGVS NC_000005.9:g.159491977T>G
CLNSRC
CLNACC RCV000454191.1,