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rs145213771

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs145213771(A;A)
Make rs145213771(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417598
GeneMHRT, MIR208B, MYH7
is asnp
is mentioned by
dbSNPrs145213771
ebirs145213771
HLIrs145213771
Exacrs145213771
Varsomers145213771
Maprs145213771
PheGenIrs145213771
hapmaprs145213771
1000 genomesrs145213771
hgdprs145213771
ensemblrs145213771
gopubmedrs145213771
geneviewrs145213771
scholarrs145213771
googlers145213771
pharmgkbrs145213771
gwascentralrs145213771
openSNPrs145213771
23andMers145213771
23andMe allrs145213771
SNP Nexus

SNPshotrs145213771
SNPdbers145213771
MSV3drs145213771
GWAS Ctlgrs145213771
Max Magnitude0
ClinVar
Risk rs145213771(A;A)
Alt rs145213771(A;A)
Reference rs145213771(G;G)
Significance Pathogenic
Disease not specified Primary familial hypertrophic cardiomyopathy
Variation info
Gene MYH7 MHRT MIR208B
CLNDBN not specified Primary familial hypertrophic cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23886807G>A
CLNSRC
CLNACC RCV000035897.3, RCV000148697.1,