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rs121434633

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121434633(A;G)
Make rs121434633(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position84955510
GeneNTRK2
is asnp
is mentioned by
dbSNPrs121434633
ebirs121434633
HLIrs121434633
Exacrs121434633
Varsomers121434633
Maprs121434633
PheGenIrs121434633
hapmaprs121434633
1000 genomesrs121434633
hgdprs121434633
ensemblrs121434633
gopubmedrs121434633
geneviewrs121434633
scholarrs121434633
googlers121434633
pharmgkbrs121434633
gwascentralrs121434633
openSNPrs121434633
23andMers121434633
23andMe allrs121434633
SNP Nexus

SNPshotrs121434633
SNPdbers121434633
MSV3drs121434633
GWAS Ctlgrs121434633
Max Magnitude0
OMIM600456
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434633(G;G)
Alt rs121434633(G;G)
Reference rs121434633(A;A)
Significance Pathogenic
Disease Obesity
Variation info
Gene NTRK2
CLNDBN Obesity, hyperphagia, and developmental delay
Reversed 0
HGVS NC_000009.11:g.87570425A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000009698.3,