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rs369751362

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369751362(C;T)
Make rs369751362(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome16
Position15720895
GeneMYH11, NDE1
is asnp
is mentioned by
dbSNPrs369751362
ebirs369751362
HLIrs369751362
Exacrs369751362
Varsomers369751362
Maprs369751362
PheGenIrs369751362
hapmaprs369751362
1000 genomesrs369751362
hgdprs369751362
ensemblrs369751362
gopubmedrs369751362
geneviewrs369751362
scholarrs369751362
googlers369751362
pharmgkbrs369751362
gwascentralrs369751362
openSNPrs369751362
23andMers369751362
23andMe allrs369751362
SNP Nexus

SNPshotrs369751362
SNPdbers369751362
MSV3drs369751362
GWAS Ctlgrs369751362
Max Magnitude0
ClinVar
Risk rs369751362(T;T)
Alt rs369751362(T;T)
Reference rs369751362(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDE1 MYH11
CLNDBN not provided
Reversed 0
HGVS NC_000016.9:g.15814752C>T
CLNSRC
CLNACC RCV000182523.2,