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rs886041091

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome9
Position84751990
GeneNTRK2
is asnp
is mentioned by
dbSNPrs886041091
dbSNP (classic)rs886041091
ClinGenrs886041091
ebirs886041091
HLIrs886041091
Exacrs886041091
Gnomadrs886041091
Varsomers886041091
LitVarrs886041091
Maprs886041091
PheGenIrs886041091
Biobankrs886041091
1000 genomesrs886041091
hgdprs886041091
ensemblrs886041091
geneviewrs886041091
scholarrs886041091
googlers886041091
pharmgkbrs886041091
gwascentralrs886041091
openSNPrs886041091
23andMers886041091
SNPshotrs886041091
SNPdbers886041091
MSV3drs886041091
GWAS Ctlgrs886041091
Max Magnitude0
ClinVar
Risk rs886041091(G;G)
Alt rs886041091(G;G)
Reference Rs886041091(A;A)
Significance Probable-Pathogenic
Disease Obesity
Variation info
Gene NTRK2
CLNDBN Obesity, hyperphagia, and developmental delay
Reversed 0
HGVS NC_000009.11:g.87366905A>G
CLNSRC
CLNACC RCV000258919.1,