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rs1064793808

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TAA;TAA) 0 common in clinvar
Chromosome18
Position62114605
GenePIGN
is asnp
is mentioned by
dbSNPrs1064793808
dbSNP (classic)rs1064793808
ClinGenrs1064793808
ebirs1064793808
HLIrs1064793808
Exacrs1064793808
Gnomadrs1064793808
Varsomers1064793808
LitVarrs1064793808
Maprs1064793808
PheGenIrs1064793808
Biobankrs1064793808
1000 genomesrs1064793808
hgdprs1064793808
ensemblrs1064793808
geneviewrs1064793808
scholarrs1064793808
googlers1064793808
pharmgkbrs1064793808
gwascentralrs1064793808
openSNPrs1064793808
23andMers1064793808
23andMe allrs1064793808
SNPshotrs1064793808
SNPdbers1064793808
MSV3drs1064793808
GWAS Ctlgrs1064793808
Max Magnitude0
ClinVar
Risk rs1064793808(AG;AG)
Alt rs1064793808(AG;AG)
Reference Rs1064793808(TAA;TAA)
Significance Pathogenic
Disease not provided
Variation info
Gene PIGN
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.59781838_59781840delTTAinsCT
CLNSRC
CLNACC RCV000481670.1,