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rs1057517888

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517888(C;T)
Make rs1057517888(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position5528120
GeneACTB
is asnp
is mentioned by
dbSNPrs1057517888
dbSNP (old)rs1057517888
ClinGenrs1057517888
ebirs1057517888
HLIrs1057517888
Exacrs1057517888
Gnomadrs1057517888
Varsomers1057517888
Maprs1057517888
PheGenIrs1057517888
Biobankrs1057517888
1000 genomesrs1057517888
hgdprs1057517888
ensemblrs1057517888
gopubmedrs1057517888
geneviewrs1057517888
scholarrs1057517888
googlers1057517888
pharmgkbrs1057517888
gwascentralrs1057517888
openSNPrs1057517888
23andMers1057517888
23andMe allrs1057517888
SNPshotrs1057517888
SNPdbers1057517888
MSV3drs1057517888
GWAS Ctlgrs1057517888
Max Magnitude0
ClinVar
Risk rs1057517888(T;T)
Alt rs1057517888(T;T)
Reference Rs1057517888(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTB
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.5567751G>A
CLNSRC
CLNACC RCV000414712.1,