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rs515726227

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs515726227(-;-)
Make rs515726227(-;TA)
Make rs515726227(TA;TA)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position4863142
GeneMSX1
is asnp
is mentioned by
dbSNPrs515726227
ebirs515726227
HLIrs515726227
Exacrs515726227
Varsomers515726227
Maprs515726227
PheGenIrs515726227
hapmaprs515726227
1000 genomesrs515726227
hgdprs515726227
ensemblrs515726227
gopubmedrs515726227
geneviewrs515726227
scholarrs515726227
googlers515726227
pharmgkbrs515726227
gwascentralrs515726227
openSNPrs515726227
23andMers515726227
23andMe allrs515726227
SNP Nexus

SNPshotrs515726227
SNPdbers515726227
MSV3drs515726227
GWAS Ctlgrs515726227
Max Magnitude0
ClinVar
Risk rs515726227(AT;AT)
Alt rs515726227(AT;AT)
Reference rs515726227(;)
Significance Pathogenic
Disease Selective tooth agenesis 1
Variation info
Gene MSX1
CLNDBN Selective tooth agenesis 1
Reversed 0
HGVS NC_000004.11:g.4864868_4864869dupTA
CLNSRC VariO
CLNACC RCV000157079.1,