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rs121908827

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121908827(C;C)
Make rs121908827(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position96254107
GeneTMEM127
is asnp
is mentioned by
dbSNPrs121908827
ebirs121908827
HLIrs121908827
Exacrs121908827
Varsomers121908827
Maprs121908827
PheGenIrs121908827
hapmaprs121908827
1000 genomesrs121908827
hgdprs121908827
ensemblrs121908827
gopubmedrs121908827
geneviewrs121908827
scholarrs121908827
googlers121908827
pharmgkbrs121908827
gwascentralrs121908827
openSNPrs121908827
23andMers121908827
23andMe allrs121908827
SNP Nexus

SNPshotrs121908827
SNPdbers121908827
MSV3drs121908827
GWAS Ctlgrs121908827
Max Magnitude0
ClinVar
Risk rs121908827(C;C)
Alt rs121908827(C;C)
Reference rs121908827(T;T)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene TMEM127
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000002.11:g.96919845A>G
CLNSRC ClinVar
CLNACC RCV000114830.1,


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

OMIM171300
Desc
Variant
Relatedalso