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rs121908821

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs121908821(G;T)
Make rs121908821(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position96254998
GeneTMEM127
is asnp
is mentioned by
dbSNPrs121908821
ebirs121908821
HLIrs121908821
Exacrs121908821
Varsomers121908821
Maprs121908821
PheGenIrs121908821
hapmaprs121908821
1000 genomesrs121908821
hgdprs121908821
ensemblrs121908821
gopubmedrs121908821
geneviewrs121908821
scholarrs121908821
googlers121908821
pharmgkbrs121908821
gwascentralrs121908821
openSNPrs121908821
23andMers121908821
23andMe allrs121908821
SNP Nexus

SNPshotrs121908821
SNPdbers121908821
MSV3drs121908821
GWAS Ctlgrs121908821
Max Magnitude0
OMIM613403
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121908821(T;T)
Alt rs121908821(T;T)
Reference rs121908821(G;G)
Significance Other
Disease Pheochromocytoma
Variation info
Gene TMEM127
CLNDBN Pheochromocytoma, susceptibility to Pheochromocytoma
Reversed 1
HGVS NC_000002.11:g.96920736C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000129.3, RCV000114824.1,


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