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rs121912556

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912556(A;A)
Make rs121912556(A;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position17816945
GeneINSL3
is asnp
is mentioned by
dbSNPrs121912556
ebirs121912556
HLIrs121912556
Exacrs121912556
Varsomers121912556
Maprs121912556
PheGenIrs121912556
hapmaprs121912556
1000 genomesrs121912556
hgdprs121912556
ensemblrs121912556
gopubmedrs121912556
geneviewrs121912556
scholarrs121912556
googlers121912556
pharmgkbrs121912556
gwascentralrs121912556
openSNPrs121912556
23andMers121912556
23andMe allrs121912556
SNP Nexus

SNPshotrs121912556
SNPdbers121912556
MSV3drs121912556
GWAS Ctlgrs121912556
Max Magnitude0
OMIM146738
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121912556(A;A)
Alt rs121912556(A;A)
Reference rs121912556(G;G)
Significance Pathogenic
Disease Cryptorchidism
Variation info
Gene INSL3
CLNDBN Cryptorchidism, unilateral or bilateral
Reversed 1
HGVS NC_000019.9:g.17927754C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015957.25,