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rs2228387

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2228387(A;A)
Make rs2228387(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position111911560
GeneCRYAB, HSPB2
is asnp
is mentioned by
dbSNPrs2228387
ebirs2228387
HLIrs2228387
Exacrs2228387
Varsomers2228387
Maprs2228387
PheGenIrs2228387
hapmaprs2228387
1000 genomesrs2228387
hgdprs2228387
ensemblrs2228387
gopubmedrs2228387
geneviewrs2228387
scholarrs2228387
googlers2228387
pharmgkbrs2228387
gwascentralrs2228387
openSNPrs2228387
23andMers2228387
23andMe allrs2228387
SNP Nexus

SNPshotrs2228387
SNPdbers2228387
MSV3drs2228387
GWAS Ctlgrs2228387
GMAF0.008264
Max Magnitude0

[PMID 21915251OA-icon.png] Association of alpha B-crystallin genotypes with oral cancer susceptibility, survival, and recurrence in taiwan


[PMID 21980040] Association of Alpha B-Crystallin (CRYAB) Genotypes with Breast Cancer Susceptibility in Taiwan


[PMID 17601350OA-icon.png] A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.


ClinVar
Risk rs2228387(A,C;A,C)
Alt rs2228387(A,C;A,C)
Reference rs2228387(G;G)
Significance Non-pathogenic
Disease not specified Dilated cardiomyopathy 1II
Variation info
Gene HSPB2-C11orf52 HSPB2 CRYAB
CLNDBN not specified Dilated cardiomyopathy 1II
Reversed 1
HGVS NC_000011.9:g.111782284C>T
CLNSRC ClinVar GeneDx
CLNACC RCV000037212.3, RCV000205646.2,