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rs119461977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs119461977(A;T)
Make rs119461977(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position89341356
GeneSECISBP2
is asnp
is mentioned by
dbSNPrs119461977
ebirs119461977
HLIrs119461977
Exacrs119461977
Varsomers119461977
Maprs119461977
PheGenIrs119461977
hapmaprs119461977
1000 genomesrs119461977
hgdprs119461977
ensemblrs119461977
gopubmedrs119461977
geneviewrs119461977
scholarrs119461977
googlers119461977
pharmgkbrs119461977
gwascentralrs119461977
openSNPrs119461977
23andMers119461977
23andMe allrs119461977
SNP Nexus

SNPshotrs119461977
SNPdbers119461977
MSV3drs119461977
GWAS Ctlgrs119461977
Max Magnitude0
OMIM607693
Desc
Variant0002
Relatedalso
ClinVar
Risk rs119461977(T;T)
Alt rs119461977(T;T)
Reference rs119461977(A;A)
Significance Pathogenic
Disease Thyroid hormone metabolism
Variation info
Gene SECISBP2
CLNDBN Thyroid hormone metabolism, abnormal
Reversed 0
HGVS NC_000009.11:g.91956271A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003054.3,