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rs1064796030

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome11
Position66866329
GenePC
is asnp
is mentioned by
dbSNPrs1064796030
dbSNP (classic)rs1064796030
ClinGenrs1064796030
ebirs1064796030
HLIrs1064796030
Exacrs1064796030
Gnomadrs1064796030
Varsomers1064796030
LitVarrs1064796030
Maprs1064796030
PheGenIrs1064796030
Biobankrs1064796030
1000 genomesrs1064796030
hgdprs1064796030
ensemblrs1064796030
geneviewrs1064796030
scholarrs1064796030
googlers1064796030
pharmgkbrs1064796030
gwascentralrs1064796030
openSNPrs1064796030
23andMers1064796030
23andMe allrs1064796030
SNPshotrs1064796030
SNPdbers1064796030
MSV3drs1064796030
GWAS Ctlgrs1064796030
Max Magnitude0
ClinVar
Risk rs1064796030(-;-)
Alt rs1064796030(-;-)
Reference Rs1064796030(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66633800delT
CLNSRC
CLNACC RCV000483564.1,