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rs121912972

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121912972(-;-)
Make rs121912972(-;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position174725004
GeneMSX2
is asnp
is mentioned by
dbSNPrs121912972
ebirs121912972
HLIrs121912972
Exacrs121912972
Varsomers121912972
Maprs121912972
PheGenIrs121912972
hapmaprs121912972
1000 genomesrs121912972
hgdprs121912972
ensemblrs121912972
gopubmedrs121912972
geneviewrs121912972
scholarrs121912972
googlers121912972
pharmgkbrs121912972
gwascentralrs121912972
openSNPrs121912972
23andMers121912972
23andMe allrs121912972
SNP Nexus

SNPshotrs121912972
SNPdbers121912972
MSV3drs121912972
GWAS Ctlgrs121912972
Max Magnitude0
OMIM123101
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121912972(;)
Alt rs121912972(;)
Reference rs121912972(G;G)
Significance Pathogenic
Disease Parietal foramina 1
Variation info
Gene MSX2
CLNDBN Parietal foramina 1
Reversed 0
HGVS NC_000005.9:g.174152007delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000018479.23,