Have questions? Visit https://www.reddit.com/r/SNPedia

rs121912548

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121912548(A;T)
Make rs121912548(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position157006595
GeneMNX1
is asnp
is mentioned by
dbSNPrs121912548
ebirs121912548
HLIrs121912548
Exacrs121912548
Varsomers121912548
Maprs121912548
PheGenIrs121912548
hapmaprs121912548
1000 genomesrs121912548
hgdprs121912548
ensemblrs121912548
gopubmedrs121912548
geneviewrs121912548
scholarrs121912548
googlers121912548
pharmgkbrs121912548
gwascentralrs121912548
openSNPrs121912548
23andMers121912548
23andMe allrs121912548
SNP Nexus

SNPshotrs121912548
SNPdbers121912548
MSV3drs121912548
GWAS Ctlgrs121912548
Max Magnitude0
OMIM142994
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121912548(T;T)
Alt rs121912548(T;T)
Reference rs121912548(A;A)
Significance Pathogenic
Disease Currarino triad
Variation info
Gene MNX1
CLNDBN Currarino triad
Reversed 1
HGVS NC_000007.13:g.156799289T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015982.25,