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

rs121908829

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908829(A;A)
Make rs121908829(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position96254078
GeneTMEM127
is asnp
is mentioned by
dbSNPrs121908829
ebirs121908829
HLIrs121908829
Exacrs121908829
Varsomers121908829
Maprs121908829
PheGenIrs121908829
hapmaprs121908829
1000 genomesrs121908829
hgdprs121908829
ensemblrs121908829
gopubmedrs121908829
geneviewrs121908829
scholarrs121908829
googlers121908829
pharmgkbrs121908829
gwascentralrs121908829
openSNPrs121908829
23andMers121908829
23andMe allrs121908829
SNP Nexus

SNPshotrs121908829
SNPdbers121908829
MSV3drs121908829
GWAS Ctlgrs121908829
Max Magnitude0
ClinVar
Risk rs121908829(A;A)
Alt rs121908829(A;A)
Reference rs121908829(G;G)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene TMEM127
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000002.11:g.96919816C>T
CLNSRC ClinVar
CLNACC RCV000114832.1,


[PMID 21156949] Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.

OMIM171300
Desc
Variant
Relatedalso