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rs886041395

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Chromosome1
Position3411770
GenePRDM16
is asnp
is mentioned by
dbSNPrs886041395
dbSNP (classic)rs886041395
ClinGenrs886041395
ebirs886041395
HLIrs886041395
Exacrs886041395
Gnomadrs886041395
Varsomers886041395
LitVarrs886041395
Maprs886041395
PheGenIrs886041395
Biobankrs886041395
1000 genomesrs886041395
hgdprs886041395
ensemblrs886041395
geneviewrs886041395
scholarrs886041395
googlers886041395
pharmgkbrs886041395
gwascentralrs886041395
openSNPrs886041395
23andMers886041395
SNPshotrs886041395
SNPdbers886041395
MSV3drs886041395
GWAS Ctlgrs886041395
Max Magnitude0
ClinVar
Risk rs886041395(C;C)
Alt rs886041395(C;C)
Reference Rs886041395(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene PRDM16
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.3328334dupC
CLNSRC
CLNACC RCV000365162.1,