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rs398122919

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122919(A;A)
Make rs398122919(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position131275746
GeneIGSF1
is asnp
is mentioned by
dbSNPrs398122919
ebirs398122919
HLIrs398122919
Exacrs398122919
Varsomers398122919
Maprs398122919
PheGenIrs398122919
hapmaprs398122919
1000 genomesrs398122919
hgdprs398122919
ensemblrs398122919
gopubmedrs398122919
geneviewrs398122919
scholarrs398122919
googlers398122919
pharmgkbrs398122919
gwascentralrs398122919
openSNPrs398122919
23andMers398122919
23andMe allrs398122919
SNP Nexus

SNPshotrs398122919
SNPdbers398122919
MSV3drs398122919
GWAS Ctlgrs398122919
Max Magnitude0
ClinVar
Risk rs398122919(A;A)
Alt rs398122919(A;A)
Reference rs398122919(G;G)
Significance Pathogenic
Disease Hypothyroidism
Variation info
Gene IGSF1
CLNDBN Hypothyroidism, central, and testicular enlargement
Reversed 1
HGVS NC_000023.10:g.130409720C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000033077.16,