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rs587776808

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(GA;GA) 0 common in clinvar
Make rs587776808(-;-)
Make rs587776808(-;C)
ReferenceGRCh38 38.1/142
Chromosome22
Position36282730
GeneMYH9
is asnp
is mentioned by
dbSNPrs587776808
ebirs587776808
HLIrs587776808
Exacrs587776808
Varsomers587776808
Maprs587776808
PheGenIrs587776808
hapmaprs587776808
1000 genomesrs587776808
hgdprs587776808
ensemblrs587776808
gopubmedrs587776808
geneviewrs587776808
scholarrs587776808
googlers587776808
pharmgkbrs587776808
gwascentralrs587776808
openSNPrs587776808
23andMers587776808
23andMe allrs587776808
SNP Nexus

SNPshotrs587776808
SNPdbers587776808
MSV3drs587776808
GWAS Ctlgrs587776808
Max Magnitude0
ClinVar
Risk rs587776808(CA,A;CA,A)
Alt rs587776808(CA,A;CA,A)
Reference rs587776808(GA;GA)
Significance Pathogenic
Disease May-Hegglin anomaly MYH9 related disorders
Variation info
Gene MYH9
CLNDBN May-Hegglin anomaly MYH9 related disorders
Reversed 1
HGVS NC_000022.10:g.36678776delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000015131.26, RCV000192271.1,