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rs119461976

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs119461976(A;A)
Make rs119461976(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position89348095
GeneSECISBP2
is asnp
is mentioned by
dbSNPrs119461976
ebirs119461976
HLIrs119461976
Exacrs119461976
Varsomers119461976
Maprs119461976
PheGenIrs119461976
hapmaprs119461976
1000 genomesrs119461976
hgdprs119461976
ensemblrs119461976
gopubmedrs119461976
geneviewrs119461976
scholarrs119461976
googlers119461976
pharmgkbrs119461976
gwascentralrs119461976
openSNPrs119461976
23andMers119461976
23andMe allrs119461976
SNP Nexus

SNPshotrs119461976
SNPdbers119461976
MSV3drs119461976
GWAS Ctlgrs119461976
Max Magnitude0
OMIM607693
Desc
Variant0001
Relatedalso
ClinVar
Risk rs119461976(A;A)
Alt rs119461976(A;A)
Reference rs119461976(G;G)
Significance Pathogenic
Disease Thyroid hormone metabolism
Variation info
Gene SECISBP2
CLNDBN Thyroid hormone metabolism, abnormal
Reversed 0
HGVS NC_000009.11:g.91963010G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003053.2,