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rs786205449

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205449(A;A)
Make rs786205449(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156879262
GeneNTRK1
is asnp
is mentioned by
dbSNPrs786205449
ebirs786205449
HLIrs786205449
Exacrs786205449
Varsomers786205449
Maprs786205449
PheGenIrs786205449
hapmaprs786205449
1000 genomesrs786205449
hgdprs786205449
ensemblrs786205449
gopubmedrs786205449
geneviewrs786205449
scholarrs786205449
googlers786205449
pharmgkbrs786205449
gwascentralrs786205449
openSNPrs786205449
23andMers786205449
23andMe allrs786205449
SNP Nexus

SNPshotrs786205449
SNPdbers786205449
MSV3drs786205449
GWAS Ctlgrs786205449
Max Magnitude0
ClinVar
Risk rs786205449(A;A)
Alt rs786205449(A;A)
Reference rs786205449(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NTRK1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156849054G>A
CLNSRC
CLNACC RCV000171160.1,