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rs387906807

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs387906807(C;C)
Make rs387906807(C;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position59231737
GeneMYO1E
is asnp
is mentioned by
dbSNPrs387906807
ebirs387906807
HLIrs387906807
Exacrs387906807
Varsomers387906807
Maprs387906807
PheGenIrs387906807
hapmaprs387906807
1000 genomesrs387906807
hgdprs387906807
ensemblrs387906807
gopubmedrs387906807
geneviewrs387906807
scholarrs387906807
googlers387906807
pharmgkbrs387906807
gwascentralrs387906807
openSNPrs387906807
23andMers387906807
23andMe allrs387906807
SNP Nexus

SNPshotrs387906807
SNPdbers387906807
MSV3drs387906807
GWAS Ctlgrs387906807
Max Magnitude0
ClinVar
Risk rs387906807(C;C)
Alt rs387906807(C;C)
Reference rs387906807(G;G)
Significance Pathogenic
Disease Focal segmental glomerulosclerosis 6
Variation info
Gene MYO1E
CLNDBN Focal segmental glomerulosclerosis 6
Reversed 1
HGVS NC_000015.9:g.59523936C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023110.2,