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rs776731688

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs776731688(A;A)
Make rs776731688(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position35577384
GenePEX12
is asnp
is mentioned by
dbSNPrs776731688
ebirs776731688
HLIrs776731688
Exacrs776731688
Varsomers776731688
Maprs776731688
PheGenIrs776731688
hapmaprs776731688
1000 genomesrs776731688
hgdprs776731688
ensemblrs776731688
gopubmedrs776731688
geneviewrs776731688
scholarrs776731688
googlers776731688
pharmgkbrs776731688
gwascentralrs776731688
openSNPrs776731688
23andMers776731688
23andMe allrs776731688
SNP Nexus

SNPshotrs776731688
SNPdbers776731688
MSV3drs776731688
GWAS Ctlgrs776731688
Max Magnitude0
ClinVar
Risk rs776731688(A;A)
Alt rs776731688(A;A)
Reference rs776731688(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PEX12
CLNDBN not provided
Reversed 0
HGVS NC_000017.10:g.33904403G>A
CLNSRC
CLNACC RCV000171254.1,