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rs1057518480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518480(G;G)
Make rs1057518480(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position25231714
GeneCRYBB2
is asnp
is mentioned by
dbSNPrs1057518480
dbSNP (old)rs1057518480
ClinGenrs1057518480
ebirs1057518480
HLIrs1057518480
Exacrs1057518480
Gnomadrs1057518480
Varsomers1057518480
Maprs1057518480
PheGenIrs1057518480
Biobankrs1057518480
1000 genomesrs1057518480
hgdprs1057518480
ensemblrs1057518480
gopubmedrs1057518480
geneviewrs1057518480
scholarrs1057518480
googlers1057518480
pharmgkbrs1057518480
gwascentralrs1057518480
openSNPrs1057518480
23andMers1057518480
23andMe allrs1057518480
SNPshotrs1057518480
SNPdbers1057518480
MSV3drs1057518480
GWAS Ctlgrs1057518480
Max Magnitude0
ClinVar
Risk rs1057518480(G;G)
Alt rs1057518480(G;G)
Reference Rs1057518480(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CRYBB2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.25627681T>G
CLNSRC
CLNACC RCV000412960.1,