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rs121908820

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908820(C;C)
Make rs121908820(C;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position96265165
GeneTMEM127
is asnp
is mentioned by
dbSNPrs121908820
ebirs121908820
HLIrs121908820
Exacrs121908820
Varsomers121908820
Maprs121908820
PheGenIrs121908820
hapmaprs121908820
1000 genomesrs121908820
hgdprs121908820
ensemblrs121908820
gopubmedrs121908820
geneviewrs121908820
scholarrs121908820
googlers121908820
pharmgkbrs121908820
gwascentralrs121908820
openSNPrs121908820
23andMers121908820
23andMe allrs121908820
SNP Nexus

SNPshotrs121908820
SNPdbers121908820
MSV3drs121908820
GWAS Ctlgrs121908820
Max Magnitude0
ClinVar
Risk rs121908820(C;C)
Alt rs121908820(C;C)
Reference rs121908820(G;G)
Significance Other
Disease Pheochromocytoma
Variation info
Gene TMEM127 CIAO1
CLNDBN Pheochromocytoma
Reversed 1
HGVS NC_000002.11:g.96930903C>G
CLNSRC ClinVar University of Washington
CLNACC RCV000114823.3,


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

OMIM171300
Desc
Variant
Relatedalso