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rs104894865

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104894865(G;T)
Make rs104894865(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position10567205
GeneMID1
is asnp
is mentioned by
dbSNPrs104894865
ebirs104894865
HLIrs104894865
Exacrs104894865
Varsomers104894865
Maprs104894865
PheGenIrs104894865
hapmaprs104894865
1000 genomesrs104894865
hgdprs104894865
ensemblrs104894865
gopubmedrs104894865
geneviewrs104894865
scholarrs104894865
googlers104894865
pharmgkbrs104894865
gwascentralrs104894865
openSNPrs104894865
23andMers104894865
23andMe allrs104894865
SNP Nexus

SNPshotrs104894865
SNPdbers104894865
MSV3drs104894865
GWAS Ctlgrs104894865
Max Magnitude0
OMIM300552
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104894865(T;T)
Alt rs104894865(T;T)
Reference rs104894865(G;G)
Significance Pathogenic
Disease Opitz-Frias syndrome
Variation info
Gene MID1
CLNDBN Opitz-Frias syndrome
Reversed 1
HGVS NC_000023.10:g.10535245C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000011556.6,