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rs397514622

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397514622(C;T)
Make rs397514622(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position131276974
GeneIGSF1
is asnp
is mentioned by
dbSNPrs397514622
ebirs397514622
HLIrs397514622
Exacrs397514622
Varsomers397514622
Maprs397514622
PheGenIrs397514622
hapmaprs397514622
1000 genomesrs397514622
hgdprs397514622
ensemblrs397514622
gopubmedrs397514622
geneviewrs397514622
scholarrs397514622
googlers397514622
pharmgkbrs397514622
gwascentralrs397514622
openSNPrs397514622
23andMers397514622
23andMe allrs397514622
SNP Nexus

SNPshotrs397514622
SNPdbers397514622
MSV3drs397514622
GWAS Ctlgrs397514622
Max Magnitude0
ClinVar
Risk rs397514622(T;T)
Alt rs397514622(T;T)
Reference rs397514622(C;C)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene IGSF1
CLNDBN Hypothyroidism, central, and testicular enlargement
Reversed 1
HGVS NC_000023.10:g.130410948G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000033079.24,