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rs7447927

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs7447927(C;G)
Make rs7447927(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position139481561
GeneTMEM173
is asnp
is mentioned by
dbSNPrs7447927
dbSNP (old)rs7447927
ClinGenrs7447927
ebirs7447927
HLIrs7447927
Exacrs7447927
Gnomadrs7447927
Varsomers7447927
Maprs7447927
PheGenIrs7447927
Biobankrs7447927
1000 genomesrs7447927
hgdprs7447927
ensemblrs7447927
gopubmedrs7447927
geneviewrs7447927
scholarrs7447927
googlers7447927
pharmgkbrs7447927
gwascentralrs7447927
openSNPrs7447927
23andMers7447927
23andMe allrs7447927
SNP Nexus

SNPshotrs7447927
SNPdbers7447927
MSV3drs7447927
GWAS Ctlgrs7447927
Max Magnitude0

[PMID 25129146OA-icon.png] Joint analysis of three genome-wide association studies of esophageal squamous cell carcinoma in Chinese populations

ClinVar
Risk rs7447927(G;G) rs7447927(T;T)
Alt rs7447927(G;G) rs7447927(T;T)
Reference Rs7447927(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene TMEM173
CLNDBN not specified
Reversed 0
HGVS NC_000005.9:g.138861146C>G
CLNSRC
CLNACC RCV000455772.1,