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rs797044804

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044804(A;T)
Make rs797044804(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position36291990
GeneMYH9
is asnp
is mentioned by
dbSNPrs797044804
ebirs797044804
HLIrs797044804
Exacrs797044804
Varsomers797044804
Maprs797044804
PheGenIrs797044804
hapmaprs797044804
1000 genomesrs797044804
hgdprs797044804
ensemblrs797044804
gopubmedrs797044804
geneviewrs797044804
scholarrs797044804
googlers797044804
pharmgkbrs797044804
gwascentralrs797044804
openSNPrs797044804
23andMers797044804
23andMe allrs797044804
SNP Nexus

SNPshotrs797044804
SNPdbers797044804
MSV3drs797044804
GWAS Ctlgrs797044804
Max Magnitude0
ClinVar
Risk rs797044804(T;T)
Alt rs797044804(T;T)
Reference rs797044804(A;A)
Significance Pathogenic
Disease MYH9 related disorders
Variation info
Gene MYH9
CLNDBN MYH9 related disorders
Reversed 1
HGVS NC_000022.10:g.36688036T>A
CLNSRC
CLNACC RCV000192270.1,