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rs1057518073

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518073(C;T)
Make rs1057518073(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position5528604
GeneACTB
is asnp
is mentioned by
dbSNPrs1057518073
dbSNP (old)rs1057518073
ClinGenrs1057518073
ebirs1057518073
HLIrs1057518073
Exacrs1057518073
Gnomadrs1057518073
Varsomers1057518073
Maprs1057518073
PheGenIrs1057518073
Biobankrs1057518073
1000 genomesrs1057518073
hgdprs1057518073
ensemblrs1057518073
gopubmedrs1057518073
geneviewrs1057518073
scholarrs1057518073
googlers1057518073
pharmgkbrs1057518073
gwascentralrs1057518073
openSNPrs1057518073
23andMers1057518073
23andMe allrs1057518073
SNPshotrs1057518073
SNPdbers1057518073
MSV3drs1057518073
GWAS Ctlgrs1057518073
Max Magnitude0
ClinVar
Risk rs1057518073(T;T)
Alt rs1057518073(T;T)
Reference Rs1057518073(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTB
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.5568235G>A
CLNSRC
CLNACC RCV000414211.1,