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rs121964867

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121964867(C;C)
Make rs121964867(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position156879234
GeneNTRK1
is asnp
is mentioned by
dbSNPrs121964867
ebirs121964867
HLIrs121964867
Exacrs121964867
Varsomers121964867
Maprs121964867
PheGenIrs121964867
hapmaprs121964867
1000 genomesrs121964867
hgdprs121964867
ensemblrs121964867
gopubmedrs121964867
geneviewrs121964867
scholarrs121964867
googlers121964867
pharmgkbrs121964867
gwascentralrs121964867
openSNPrs121964867
23andMers121964867
23andMe allrs121964867
SNP Nexus

SNPshotrs121964867
SNPdbers121964867
MSV3drs121964867
GWAS Ctlgrs121964867
Max Magnitude0
OMIM191315
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121964867(C;C)
Alt rs121964867(C;C)
Reference rs121964867(T;T)
Significance Untested
Disease Familial medullary thyroid carcinoma
Variation info
Gene NTRK1
CLNDBN Familial medullary thyroid carcinoma
Reversed 0
HGVS NC_000001.10:g.156849026T>C
CLNSRC OMIM Allelic Variant
CLNACC SCV000033347.1,