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rs886041327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Chromosome16
Position29813377
GenePRRT2
is asnp
is mentioned by
dbSNPrs886041327
dbSNP (classic)rs886041327
ClinGenrs886041327
ebirs886041327
HLIrs886041327
Exacrs886041327
Gnomadrs886041327
Varsomers886041327
LitVarrs886041327
Maprs886041327
PheGenIrs886041327
Biobankrs886041327
1000 genomesrs886041327
hgdprs886041327
ensemblrs886041327
geneviewrs886041327
scholarrs886041327
googlers886041327
pharmgkbrs886041327
gwascentralrs886041327
openSNPrs886041327
23andMers886041327
23andMe allrs886041327
SNPshotrs886041327
SNPdbers886041327
MSV3drs886041327
GWAS Ctlgrs886041327
Max Magnitude0
ClinVar
Risk rs886041327(-;-)
Alt rs886041327(-;-)
Reference Rs886041327(AC;AC)
Significance Pathogenic
Disease not provided
Variation info
Gene PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29824698_29824699delCA
CLNSRC
CLNACC RCV000278799.1,