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rs121912549

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912549(G;T)
Make rs121912549(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position157006487
GeneMNX1
is asnp
is mentioned by
dbSNPrs121912549
ebirs121912549
HLIrs121912549
Exacrs121912549
Varsomers121912549
Maprs121912549
PheGenIrs121912549
hapmaprs121912549
1000 genomesrs121912549
hgdprs121912549
ensemblrs121912549
gopubmedrs121912549
geneviewrs121912549
scholarrs121912549
googlers121912549
pharmgkbrs121912549
gwascentralrs121912549
openSNPrs121912549
23andMers121912549
23andMe allrs121912549
SNP Nexus

SNPshotrs121912549
SNPdbers121912549
MSV3drs121912549
GWAS Ctlgrs121912549
Max Magnitude0
OMIM142994
Desc
Variant0010
Relatedalso
ClinVar
Risk rs121912549(T;T)
Alt rs121912549(T;T)
Reference rs121912549(G;G)
Significance Pathogenic
Disease Currarino triad
Variation info
Gene MNX1
CLNDBN Currarino triad
Reversed 1
HGVS NC_000007.13:g.156799181C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015984.25,