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rs1064794861

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome17
Position16325863
GenePIGL
is asnp
is mentioned by
dbSNPrs1064794861
dbSNP (old)rs1064794861
ClinGenrs1064794861
ebirs1064794861
HLIrs1064794861
Exacrs1064794861
Gnomadrs1064794861
Varsomers1064794861
Maprs1064794861
PheGenIrs1064794861
Biobankrs1064794861
1000 genomesrs1064794861
hgdprs1064794861
ensemblrs1064794861
gopubmedrs1064794861
geneviewrs1064794861
scholarrs1064794861
googlers1064794861
pharmgkbrs1064794861
gwascentralrs1064794861
openSNPrs1064794861
23andMers1064794861
23andMe allrs1064794861
SNPshotrs1064794861
SNPdbers1064794861
MSV3drs1064794861
GWAS Ctlgrs1064794861
Max Magnitude0
ClinVar
Risk rs1064794861(-;-)
Alt rs1064794861(-;-)
Reference Rs1064794861(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PIGL
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.16229177delC
CLNSRC
CLNACC RCV000484412.1,