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rs80338830

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80338830(G;T)
Make rs80338830(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position36295068
GeneMYH9
is asnp
is mentioned by
dbSNPrs80338830
ebirs80338830
HLIrs80338830
Exacrs80338830
Varsomers80338830
Maprs80338830
PheGenIrs80338830
hapmaprs80338830
1000 genomesrs80338830
hgdprs80338830
ensemblrs80338830
gopubmedrs80338830
geneviewrs80338830
scholarrs80338830
googlers80338830
pharmgkbrs80338830
gwascentralrs80338830
openSNPrs80338830
23andMers80338830
23andMe allrs80338830
SNP Nexus

SNPshotrs80338830
SNPdbers80338830
MSV3drs80338830
GWAS Ctlgrs80338830
Max Magnitude0
ClinVar
Risk rs80338830(T;T)
Alt rs80338830(T;T)
Reference rs80338830(G;G)
Significance Pathogenic
Disease MYH9 related disorders
Variation info
Gene MYH9
CLNDBN MYH9 related disorders
Reversed 1
HGVS NC_000022.10:g.36691114C>A
CLNSRC ClinVar GeneReviews
CLNACC RCV000032221.1,