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rs6977660

From SNPedia

Orientationplus
Stabilizedplus
Make rs6977660(C;C)
Make rs6977660(C;T)
Make rs6977660(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position19765857
GeneTMEM196
is asnp
is mentioned by
dbSNPrs6977660
ebirs6977660
HLIrs6977660
Exacrs6977660
Varsomers6977660
Maprs6977660
PheGenIrs6977660
hapmaprs6977660
1000 genomesrs6977660
hgdprs6977660
ensemblrs6977660
gopubmedrs6977660
geneviewrs6977660
scholarrs6977660
googlers6977660
pharmgkbrs6977660
gwascentralrs6977660
openSNPrs6977660
23andMers6977660
23andMe allrs6977660
SNP Nexus

SNPshotrs6977660
SNPdbers6977660
MSV3drs6977660
GWAS Ctlgrs6977660
GMAF0.3499
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs6977660
PubMedID [PMID 17903292OA-icon.png]
Condition Thyroid stimulating hormone
Gene Intergenic
Risk Allele
pValue 4.00E-006
OR NA
95% CI



GET Evidence
rs6977660
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.3125
summary