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rs886041579

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Chromosome16
Position29813264
GenePRRT2
is asnp
is mentioned by
dbSNPrs886041579
dbSNP (classic)rs886041579
ClinGenrs886041579
ebirs886041579
HLIrs886041579
Exacrs886041579
Gnomadrs886041579
Varsomers886041579
LitVarrs886041579
Maprs886041579
PheGenIrs886041579
Biobankrs886041579
1000 genomesrs886041579
hgdprs886041579
ensemblrs886041579
geneviewrs886041579
scholarrs886041579
googlers886041579
pharmgkbrs886041579
gwascentralrs886041579
openSNPrs886041579
23andMers886041579
23andMe allrs886041579
SNPshotrs886041579
SNPdbers886041579
MSV3drs886041579
GWAS Ctlgrs886041579
Max Magnitude0
ClinVar
Risk rs886041579(-;-)
Alt rs886041579(-;-)
Reference Rs886041579(AA;AA)
Significance Pathogenic
Disease not provided
Variation info
Gene PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29824585_29824586delAA
CLNSRC
CLNACC RCV000334772.1,