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rs1064796768

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome16
Position14628177
GenePARN
is asnp
is mentioned by
dbSNPrs1064796768
dbSNP (old)rs1064796768
ClinGenrs1064796768
ebirs1064796768
HLIrs1064796768
Exacrs1064796768
Gnomadrs1064796768
Varsomers1064796768
Maprs1064796768
PheGenIrs1064796768
Biobankrs1064796768
1000 genomesrs1064796768
hgdprs1064796768
ensemblrs1064796768
gopubmedrs1064796768
geneviewrs1064796768
scholarrs1064796768
googlers1064796768
pharmgkbrs1064796768
gwascentralrs1064796768
openSNPrs1064796768
23andMers1064796768
23andMe allrs1064796768
SNPshotrs1064796768
SNPdbers1064796768
MSV3drs1064796768
GWAS Ctlgrs1064796768
Max Magnitude0
ClinVar
Risk rs1064796768(T;T)
Alt rs1064796768(T;T)
Reference Rs1064796768(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene PARN
CLNDBN not provided
Reversed 1
HGVS NC_000016.9:g.14722034T>A
CLNSRC
CLNACC RCV000484532.1,