Have questions? Visit https://www.reddit.com/r/SNPedia

rs879253889

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs879253889(C;T)
Make rs879253889(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome1
Position156868201
GeneNTRK1
is asnp
is mentioned by
dbSNPrs879253889
dbSNP (classic)rs879253889
ClinGenrs879253889
ebirs879253889
HLIrs879253889
Exacrs879253889
Gnomadrs879253889
Varsomers879253889
LitVarrs879253889
Maprs879253889
PheGenIrs879253889
Biobankrs879253889
1000 genomesrs879253889
hgdprs879253889
ensemblrs879253889
geneviewrs879253889
scholarrs879253889
googlers879253889
pharmgkbrs879253889
gwascentralrs879253889
openSNPrs879253889
23andMers879253889
SNPshotrs879253889
SNPdbers879253889
MSV3drs879253889
GWAS Ctlgrs879253889
Max Magnitude0
ClinVar
Risk rs879253889(T;T)
Alt rs879253889(T;T)
Reference Rs879253889(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene NTRK1
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156837993C>T
CLNSRC
CLNACC RCV000236167.1,