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rs187225056

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs187225056(A;A)
Make rs187225056(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome16
Position1495402
GeneTELO2
is asnp
is mentioned by
dbSNPrs187225056
dbSNP (old)rs187225056
ClinGenrs187225056
ebirs187225056
HLIrs187225056
Exacrs187225056
Gnomadrs187225056
Varsomers187225056
Maprs187225056
PheGenIrs187225056
Biobankrs187225056
1000 genomesrs187225056
hgdprs187225056
ensemblrs187225056
gopubmedrs187225056
geneviewrs187225056
scholarrs187225056
googlers187225056
pharmgkbrs187225056
gwascentralrs187225056
openSNPrs187225056
23andMers187225056
23andMe allrs187225056
SNPshotrs187225056
SNPdbers187225056
MSV3drs187225056
GWAS Ctlgrs187225056
Max Magnitude0
ClinVar
Risk rs187225056(A;A)
Alt rs187225056(A;A)
Reference Rs187225056(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TELO2
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.1545403G>A
CLNSRC
CLNACC RCV000486946.1,