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rs121908826

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121908826(A;C)
Make rs121908826(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position96254117
GeneTMEM127
is asnp
is mentioned by
dbSNPrs121908826
ebirs121908826
HLIrs121908826
Exacrs121908826
Varsomers121908826
Maprs121908826
PheGenIrs121908826
hapmaprs121908826
1000 genomesrs121908826
hgdprs121908826
ensemblrs121908826
gopubmedrs121908826
geneviewrs121908826
scholarrs121908826
googlers121908826
pharmgkbrs121908826
gwascentralrs121908826
openSNPrs121908826
23andMers121908826
23andMe allrs121908826
SNP Nexus

SNPshotrs121908826
SNPdbers121908826
MSV3drs121908826
GWAS Ctlgrs121908826
Max Magnitude0
OMIM613403
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121908826(C;C)
Alt rs121908826(C;C)
Reference rs121908826(A;A)
Significance Other
Disease Pheochromocytoma
Variation info
Gene TMEM127
CLNDBN Pheochromocytoma, susceptibility to Pheochromocytoma
Reversed 1
HGVS NC_000002.11:g.96919855T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000000127.3, RCV000114829.1,


[PMID 20154675OA-icon.png] Germline mutations in TMEM127 confer susceptibility to pheochromocytoma.