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rs121912546

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121912546(C;T)
Make rs121912546(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position157006556
GeneMNX1
is asnp
is mentioned by
dbSNPrs121912546
ebirs121912546
HLIrs121912546
Exacrs121912546
Varsomers121912546
Maprs121912546
PheGenIrs121912546
hapmaprs121912546
1000 genomesrs121912546
hgdprs121912546
ensemblrs121912546
gopubmedrs121912546
geneviewrs121912546
scholarrs121912546
googlers121912546
pharmgkbrs121912546
gwascentralrs121912546
openSNPrs121912546
23andMers121912546
23andMe allrs121912546
SNP Nexus

SNPshotrs121912546
SNPdbers121912546
MSV3drs121912546
GWAS Ctlgrs121912546
Max Magnitude0
OMIM142994
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121912546(T;T)
Alt rs121912546(T;T)
Reference rs121912546(C;C)
Significance Pathogenic
Disease Currarino triad
Variation info
Gene MNX1
CLNDBN Currarino triad
Reversed 1
HGVS NC_000007.13:g.156799250G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015976.21,