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rs1085307663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position3411656
GenePRDM16
is asnp
is mentioned by
dbSNPrs1085307663
dbSNP (old)rs1085307663
ClinGenrs1085307663
ebirs1085307663
HLIrs1085307663
Exacrs1085307663
Gnomadrs1085307663
Varsomers1085307663
Maprs1085307663
PheGenIrs1085307663
Biobankrs1085307663
1000 genomesrs1085307663
hgdprs1085307663
ensemblrs1085307663
gopubmedrs1085307663
geneviewrs1085307663
scholarrs1085307663
googlers1085307663
pharmgkbrs1085307663
gwascentralrs1085307663
openSNPrs1085307663
23andMers1085307663
23andMe allrs1085307663
SNPshotrs1085307663
SNPdbers1085307663
MSV3drs1085307663
GWAS Ctlgrs1085307663
Max Magnitude0
ClinVar
Risk rs1085307663(-;-)
Alt rs1085307663(-;-)
Reference Rs1085307663(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PRDM16
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.3328220delG
CLNSRC
CLNACC RCV000489128.1,