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rs398122886

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs398122886(C;T)
Make rs398122886(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position17817033
GeneINSL3
is asnp
is mentioned by
dbSNPrs398122886
ebirs398122886
HLIrs398122886
Exacrs398122886
Varsomers398122886
Maprs398122886
PheGenIrs398122886
hapmaprs398122886
1000 genomesrs398122886
hgdprs398122886
ensemblrs398122886
gopubmedrs398122886
geneviewrs398122886
scholarrs398122886
googlers398122886
pharmgkbrs398122886
gwascentralrs398122886
openSNPrs398122886
23andMers398122886
23andMe allrs398122886
SNP Nexus

SNPshotrs398122886
SNPdbers398122886
MSV3drs398122886
GWAS Ctlgrs398122886
Max Magnitude0
ClinVar
Risk rs398122886(T;T)
Alt rs398122886(T;T)
Reference rs398122886(C;C)
Significance Pathogenic
Disease Cryptorchidism
Variation info
Gene INSL3
CLNDBN Cryptorchidism, unilateral or bilateral
Reversed 1
HGVS NC_000019.9:g.17927842G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030739.25,