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rs397516234

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CCATCG;CCATCG) 0 common in clinvar
Make rs397516234(-;-)
Make rs397516234(-;CCATCG)
ReferenceGRCh38 38.1/141
Chromosome14
Position23415766
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516234
ebirs397516234
HLIrs397516234
Exacrs397516234
Varsomers397516234
Maprs397516234
PheGenIrs397516234
hapmaprs397516234
1000 genomesrs397516234
hgdprs397516234
ensemblrs397516234
gopubmedrs397516234
geneviewrs397516234
scholarrs397516234
googlers397516234
pharmgkbrs397516234
gwascentralrs397516234
openSNPrs397516234
23andMers397516234
23andMe allrs397516234
SNP Nexus

SNPshotrs397516234
SNPdbers397516234
MSV3drs397516234
GWAS Ctlgrs397516234
Max Magnitude0
ClinVar
Risk rs397516234(;)
Alt rs397516234(;)
Reference rs397516234(CCATCG;CCATCG)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23884975_23884980delCGATGG
CLNSRC ClinVar
CLNACC RCV000035945.3,