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rs398122921

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs398122921(-;-)
Make rs398122921(-;T)
Make rs398122921(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position131274768
GeneIGSF1
is asnp
is mentioned by
dbSNPrs398122921
ebirs398122921
HLIrs398122921
Exacrs398122921
Varsomers398122921
Maprs398122921
PheGenIrs398122921
hapmaprs398122921
1000 genomesrs398122921
hgdprs398122921
ensemblrs398122921
gopubmedrs398122921
geneviewrs398122921
scholarrs398122921
googlers398122921
pharmgkbrs398122921
gwascentralrs398122921
openSNPrs398122921
23andMers398122921
23andMe allrs398122921
SNP Nexus

SNPshotrs398122921
SNPdbers398122921
MSV3drs398122921
GWAS Ctlgrs398122921
Max Magnitude0
ClinVar
Risk rs398122921(T;T)
Alt rs398122921(T;T)
Reference rs398122921(;)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene IGSF1
CLNDBN Hypothyroidism, central, and testicular enlargement
Reversed 1
HGVS NC_000023.10:g.130408743dupA
CLNSRC OMIM Allelic Variant
CLNACC RCV000033080.23,