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rs201895208

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201895208(G;T)
Make rs201895208(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417616
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs201895208
ebirs201895208
HLIrs201895208
Exacrs201895208
Varsomers201895208
Maprs201895208
PheGenIrs201895208
hapmaprs201895208
1000 genomesrs201895208
hgdprs201895208
ensemblrs201895208
gopubmedrs201895208
geneviewrs201895208
scholarrs201895208
googlers201895208
pharmgkbrs201895208
gwascentralrs201895208
openSNPrs201895208
23andMers201895208
23andMe allrs201895208
SNP Nexus

SNPshotrs201895208
SNPdbers201895208
MSV3drs201895208
GWAS Ctlgrs201895208
Max Magnitude0
ClinVar
Risk rs201895208(T;T)
Alt rs201895208(T;T)
Reference rs201895208(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7 MHRT MIR208B
CLNDBN Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23886825G>T
CLNSRC
CLNACC RCV000171840.1,