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rs1085308029

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome9
Position84752019
GeneNTRK2
is asnp
is mentioned by
dbSNPrs1085308029
dbSNP (classic)rs1085308029
ClinGenrs1085308029
ebirs1085308029
HLIrs1085308029
Exacrs1085308029
Gnomadrs1085308029
Varsomers1085308029
LitVarrs1085308029
Maprs1085308029
PheGenIrs1085308029
Biobankrs1085308029
1000 genomesrs1085308029
hgdprs1085308029
ensemblrs1085308029
geneviewrs1085308029
scholarrs1085308029
googlers1085308029
pharmgkbrs1085308029
gwascentralrs1085308029
openSNPrs1085308029
23andMers1085308029
23andMe allrs1085308029
SNPshotrs1085308029
SNPdbers1085308029
MSV3drs1085308029
GWAS Ctlgrs1085308029
Max Magnitude0
ClinVar
Risk rs1085308029(T;T)
Alt rs1085308029(T;T)
Reference Rs1085308029(G;G)
Significance Pathogenic
Disease Obesity
Variation info
Gene NTRK2
CLNDBN Obesity, hyperphagia, and developmental delay
Reversed 0
HGVS NC_000009.11:g.87366934G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000490246.1,