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rs1064796229

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(GTG;GTG) 0 common in clinvar
Chromosome17
Position2665456
GenePAFAH1B1
is asnp
is mentioned by
dbSNPrs1064796229
dbSNP (old)rs1064796229
ClinGenrs1064796229
ebirs1064796229
HLIrs1064796229
Exacrs1064796229
Gnomadrs1064796229
Varsomers1064796229
Maprs1064796229
PheGenIrs1064796229
Biobankrs1064796229
1000 genomesrs1064796229
hgdprs1064796229
ensemblrs1064796229
gopubmedrs1064796229
geneviewrs1064796229
scholarrs1064796229
googlers1064796229
pharmgkbrs1064796229
gwascentralrs1064796229
openSNPrs1064796229
23andMers1064796229
23andMe allrs1064796229
SNPshotrs1064796229
SNPdbers1064796229
MSV3drs1064796229
GWAS Ctlgrs1064796229
Max Magnitude0
ClinVar
Risk rs1064796229(-;-)
Alt rs1064796229(-;-)
Reference Rs1064796229(GTG;GTG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PAFAH1B1
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.2568750_2568752delGGT
CLNSRC
CLNACC RCV000482585.1,