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rs730880269

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880269(A;A)
Make rs730880269(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position89338609
GeneSECISBP2
is asnp
is mentioned by
dbSNPrs730880269
ebirs730880269
HLIrs730880269
Exacrs730880269
Varsomers730880269
Maprs730880269
PheGenIrs730880269
hapmaprs730880269
1000 genomesrs730880269
hgdprs730880269
ensemblrs730880269
gopubmedrs730880269
geneviewrs730880269
scholarrs730880269
googlers730880269
pharmgkbrs730880269
gwascentralrs730880269
openSNPrs730880269
23andMers730880269
23andMe allrs730880269
SNP Nexus

SNPshotrs730880269
SNPdbers730880269
MSV3drs730880269
GWAS Ctlgrs730880269
Max Magnitude0
ClinVar
Risk rs730880269(A;A)
Alt rs730880269(A;A)
Reference rs730880269(G;G)
Significance Pathogenic
Disease Thyroid hormone metabolism
Variation info
Gene SECISBP2
CLNDBN Thyroid hormone metabolism, abnormal
Reversed 0
HGVS NC_000009.11:g.91953524G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003055.3,