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rs141638421

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141638421(C;T)
Make rs141638421(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position111908822
GeneCRYAB
is asnp
is mentioned by
dbSNPrs141638421
ebirs141638421
HLIrs141638421
Exacrs141638421
Varsomers141638421
Maprs141638421
PheGenIrs141638421
hapmaprs141638421
1000 genomesrs141638421
hgdprs141638421
ensemblrs141638421
gopubmedrs141638421
geneviewrs141638421
scholarrs141638421
googlers141638421
pharmgkbrs141638421
gwascentralrs141638421
openSNPrs141638421
23andMers141638421
23andMe allrs141638421
SNP Nexus

SNPshotrs141638421
SNPdbers141638421
MSV3drs141638421
GWAS Ctlgrs141638421
Max Magnitude0
ClinVar
Risk rs141638421(T;T)
Alt rs141638421(T;T)
Reference rs141638421(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1II
Variation info
Gene CRYAB
CLNDBN Dilated cardiomyopathy 1II
Reversed 0
HGVS NC_000011.9:g.111779546C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000034838.28,