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rs201307101

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201307101(A;A)
Make rs201307101(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417295
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs201307101
ebirs201307101
HLIrs201307101
Exacrs201307101
Varsomers201307101
Maprs201307101
PheGenIrs201307101
hapmaprs201307101
1000 genomesrs201307101
hgdprs201307101
ensemblrs201307101
gopubmedrs201307101
geneviewrs201307101
scholarrs201307101
googlers201307101
pharmgkbrs201307101
gwascentralrs201307101
openSNPrs201307101
23andMers201307101
23andMe allrs201307101
SNP Nexus

SNPshotrs201307101
SNPdbers201307101
MSV3drs201307101
GWAS Ctlgrs201307101
Max Magnitude0
ClinVar
Risk rs201307101(A,T;A,T)
Alt rs201307101(A,T;A,T)
Reference rs201307101(C;C)
Significance Other
Disease not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1 not provided
Variation info
Gene MYH7 MHRT
CLNDBN not specified Primary familial hypertrophic cardiomyopathy Familial hypertrophic cardiomyopathy 1 not provided
Reversed 0
HGVS NC_000014.8:g.23886504C>A
CLNSRC Centenary Institute
CLNACC RCV000035906.5, RCV000148704.1, RCV000162336.1, RCV000177508.1,