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rs886041735

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome16
Position29813261
GenePRRT2
is asnp
is mentioned by
dbSNPrs886041735
dbSNP (classic)rs886041735
ClinGenrs886041735
ebirs886041735
HLIrs886041735
Exacrs886041735
Gnomadrs886041735
Varsomers886041735
LitVarrs886041735
Maprs886041735
PheGenIrs886041735
Biobankrs886041735
1000 genomesrs886041735
hgdprs886041735
ensemblrs886041735
geneviewrs886041735
scholarrs886041735
googlers886041735
pharmgkbrs886041735
gwascentralrs886041735
openSNPrs886041735
23andMers886041735
23andMe allrs886041735
SNPshotrs886041735
SNPdbers886041735
MSV3drs886041735
GWAS Ctlgrs886041735
Max Magnitude0
ClinVar
Risk rs886041735(CCAAGGCTGGGCTGGCT;CCAAGGCTGGGCTGGCT)
Alt rs886041735(CCAAGGCTGGGCTGGCT;CCAAGGCTGGGCTGGCT)
Reference Rs886041735(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PRRT2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.29824566_29824582dup17
CLNSRC
CLNACC RCV000311228.1,