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rs886042013

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome16
Position29813378
GenePRRT2
is asnp
is mentioned by
dbSNPrs886042013
dbSNP (classic)rs886042013
ClinGenrs886042013
ebirs886042013
HLIrs886042013
Exacrs886042013
Gnomadrs886042013
Varsomers886042013
LitVarrs886042013
Maprs886042013
PheGenIrs886042013
Biobankrs886042013
1000 genomesrs886042013
hgdprs886042013
ensemblrs886042013
geneviewrs886042013
scholarrs886042013
googlers886042013
pharmgkbrs886042013
gwascentralrs886042013
openSNPrs886042013
23andMers886042013
23andMe allrs886042013
SNPshotrs886042013
SNPdbers886042013
MSV3drs886042013
GWAS Ctlgrs886042013
Max Magnitude0
ClinVar
Risk rs886042013(-;-)
Alt rs886042013(-;-)
Reference Rs886042013(AG;AG)
Significance Pathogenic
Disease not provided
Variation info
Gene PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29824699_29824700delAG
CLNSRC
CLNACC RCV000378110.1,