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rs1060499763

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1060499763(G;G)
Make rs1060499763(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position62140447
GenePIGN
is asnp
is mentioned by
dbSNPrs1060499763
dbSNP (old)rs1060499763
ClinGenrs1060499763
ebirs1060499763
HLIrs1060499763
Exacrs1060499763
Gnomadrs1060499763
Varsomers1060499763
Maprs1060499763
PheGenIrs1060499763
Biobankrs1060499763
1000 genomesrs1060499763
hgdprs1060499763
ensemblrs1060499763
gopubmedrs1060499763
geneviewrs1060499763
scholarrs1060499763
googlers1060499763
pharmgkbrs1060499763
gwascentralrs1060499763
openSNPrs1060499763
23andMers1060499763
23andMe allrs1060499763
SNPshotrs1060499763
SNPdbers1060499763
MSV3drs1060499763
GWAS Ctlgrs1060499763
Max Magnitude0
ClinVar
Risk rs1060499763(G;G)
Alt rs1060499763(G;G)
Reference Rs1060499763(T;T)
Significance Probable-Pathogenic
Disease Abnormality of brain morphology
Variation info
Gene PIGN
CLNDBN Abnormality of brain morphology
Reversed 1
HGVS NC_000018.9:g.59807680A>C
CLNSRC
CLNACC RCV000454324.1,