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rs2070894

From SNPedia

Orientationminus
Stabilizedminus
Make rs2070894(C;C)
Make rs2070894(C;T)
Make rs2070894(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position111910113
GeneCRYAB
is asnp
is mentioned by
dbSNPrs2070894
dbSNP (classic)rs2070894
ClinGenrs2070894
ebirs2070894
HLIrs2070894
Exacrs2070894
Gnomadrs2070894
Varsomers2070894
LitVarrs2070894
Maprs2070894
PheGenIrs2070894
Biobankrs2070894
1000 genomesrs2070894
hgdprs2070894
ensemblrs2070894
geneviewrs2070894
scholarrs2070894
googlers2070894
pharmgkbrs2070894
gwascentralrs2070894
openSNPrs2070894
23andMers2070894
SNPshotrs2070894
SNPdbers2070894
MSV3drs2070894
GWAS Ctlgrs2070894
GMAF0.2626
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[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 19503744OA-icon.png] An alphaA-crystallin gene mutation, Arg12Cys, causing inherited cataract-microcornea exhibits an altered heat-shock response.


[PMID 19668596OA-icon.png] A novel gammaD-crystallin mutation causes mild changes in protein properties but leads to congenital coralliform cataract.