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rs28928890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs28928890(A;T)
Make rs28928890(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position4860150
GeneMSX1
is asnp
is mentioned by
dbSNPrs28928890
ebirs28928890
HLIrs28928890
Exacrs28928890
Varsomers28928890
Maprs28928890
PheGenIrs28928890
hapmaprs28928890
1000 genomesrs28928890
hgdprs28928890
ensemblrs28928890
gopubmedrs28928890
geneviewrs28928890
scholarrs28928890
googlers28928890
pharmgkbrs28928890
gwascentralrs28928890
openSNPrs28928890
23andMers28928890
23andMe allrs28928890
SNP Nexus

SNPshotrs28928890
SNPdbers28928890
MSV3drs28928890
GWAS Ctlgrs28928890
Max Magnitude0
OMIM142983
DescOROFACIAL CLEFT 5
Variant0004
Relatedalso
Neighborrs28933081
Distance114


ClinVar
Risk rs28928890(T;T)
Alt rs28928890(T;T)
Reference rs28928890(A;A)
Significance Pathogenic
Disease Orofacial cleft 5
Variation info
Gene MSX1
CLNDBN Orofacial cleft 5
Reversed 0
HGVS NC_000004.11:g.4861877A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016012.25,