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

rs786200982

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786200982(-;-)
Make rs786200982(-;TGAT)
Make rs786200982(TGAT;TGAT)
ReferenceGRCh38.p2 38.2/146
ChromosomeX
Position10459787
GeneMID1
is asnp
is mentioned by
dbSNPrs786200982
ebirs786200982
HLIrs786200982
Exacrs786200982
Varsomers786200982
Maprs786200982
PheGenIrs786200982
hapmaprs786200982
1000 genomesrs786200982
hgdprs786200982
ensemblrs786200982
gopubmedrs786200982
geneviewrs786200982
scholarrs786200982
googlers786200982
pharmgkbrs786200982
gwascentralrs786200982
openSNPrs786200982
23andMers786200982
23andMe allrs786200982
SNP Nexus

SNPshotrs786200982
SNPdbers786200982
MSV3drs786200982
GWAS Ctlgrs786200982
Max Magnitude0
ClinVar
Risk rs786200982(TGAT;TGAT)
Alt rs786200982(TGAT;TGAT)
Reference rs786200982(;)
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.10427828_10427831dupATCA
CLNSRC
CLNACC RCV000153501.2, RCV000180150.1,