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

rs398123343

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123343(-;-)
Make rs398123343(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position10495665
GeneMID1
is asnp
is mentioned by
dbSNPrs398123343
ebirs398123343
HLIrs398123343
Exacrs398123343
Varsomers398123343
Maprs398123343
PheGenIrs398123343
hapmaprs398123343
1000 genomesrs398123343
hgdprs398123343
ensemblrs398123343
gopubmedrs398123343
geneviewrs398123343
scholarrs398123343
googlers398123343
pharmgkbrs398123343
gwascentralrs398123343
openSNPrs398123343
23andMers398123343
23andMe allrs398123343
SNP Nexus

SNPshotrs398123343
SNPdbers398123343
MSV3drs398123343
GWAS Ctlgrs398123343
Max Magnitude0
ClinVar
Risk rs398123343(;)
Alt rs398123343(;)
Reference rs398123343(A;A)
Significance Pathogenic
Disease not provided Opitz-Frias syndrome
Variation info
Gene MID1
CLNDBN not provided Opitz-Frias syndrome
Reversed 1
HGVS NC_000023.10:g.10463705delT
CLNSRC ClinVar
CLNACC RCV000078682.3, RCV000178081.1,