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rs1064795400

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position16233997
GenePIGL
is asnp
is mentioned by
dbSNPrs1064795400
dbSNP (old)rs1064795400
ClinGenrs1064795400
ebirs1064795400
HLIrs1064795400
Exacrs1064795400
Gnomadrs1064795400
Varsomers1064795400
Maprs1064795400
PheGenIrs1064795400
Biobankrs1064795400
1000 genomesrs1064795400
hgdprs1064795400
ensemblrs1064795400
gopubmedrs1064795400
geneviewrs1064795400
scholarrs1064795400
googlers1064795400
pharmgkbrs1064795400
gwascentralrs1064795400
openSNPrs1064795400
23andMers1064795400
23andMe allrs1064795400
SNPshotrs1064795400
SNPdbers1064795400
MSV3drs1064795400
GWAS Ctlgrs1064795400
Max Magnitude0
ClinVar
Risk rs1064795400(T;T)
Alt rs1064795400(T;T)
Reference Rs1064795400(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PIGL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.16137311C>T
CLNSRC
CLNACC RCV000481931.1,