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rs121908825

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908825(G;T)
Make rs121908825(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position96254832
GeneTMEM127
is asnp
is mentioned by
dbSNPrs121908825
ebirs121908825
HLIrs121908825
Exacrs121908825
Varsomers121908825
Maprs121908825
PheGenIrs121908825
hapmaprs121908825
1000 genomesrs121908825
hgdprs121908825
ensemblrs121908825
gopubmedrs121908825
geneviewrs121908825
scholarrs121908825
googlers121908825
pharmgkbrs121908825
gwascentralrs121908825
openSNPrs121908825
23andMers121908825
23andMe allrs121908825
SNP Nexus

SNPshotrs121908825
SNPdbers121908825
MSV3drs121908825
GWAS Ctlgrs121908825
Max Magnitude0
ClinVar
Risk rs121908825(T;T)
Alt rs121908825(T;T)
Reference rs121908825(G;G)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene TMEM127
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000002.11:g.96920570C>A
CLNSRC ClinVar
CLNACC RCV000114828.1,


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

OMIM171300
Desc
Variant
Relatedalso