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rs45442096

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45442096(A;A)
Make rs45442096(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416102
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs45442096
ebirs45442096
HLIrs45442096
Exacrs45442096
Varsomers45442096
Maprs45442096
PheGenIrs45442096
hapmaprs45442096
1000 genomesrs45442096
hgdprs45442096
ensemblrs45442096
gopubmedrs45442096
geneviewrs45442096
scholarrs45442096
googlers45442096
pharmgkbrs45442096
gwascentralrs45442096
openSNPrs45442096
23andMers45442096
23andMe allrs45442096
SNP Nexus

SNPshotrs45442096
SNPdbers45442096
MSV3drs45442096
GWAS Ctlgrs45442096
Max Magnitude0
ClinVar
Risk rs45442096(A;A)
Alt rs45442096(A;A)
Reference rs45442096(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23885311C>T
CLNSRC
CLNACC RCV000158674.2,