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rs1057518071

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518071(C;G)
Make rs1057518071(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position5528467
GeneACTB
is asnp
is mentioned by
dbSNPrs1057518071
dbSNP (old)rs1057518071
ClinGenrs1057518071
ebirs1057518071
HLIrs1057518071
Exacrs1057518071
Gnomadrs1057518071
Varsomers1057518071
Maprs1057518071
PheGenIrs1057518071
Biobankrs1057518071
1000 genomesrs1057518071
hgdprs1057518071
ensemblrs1057518071
gopubmedrs1057518071
geneviewrs1057518071
scholarrs1057518071
googlers1057518071
pharmgkbrs1057518071
gwascentralrs1057518071
openSNPrs1057518071
23andMers1057518071
23andMe allrs1057518071
SNPshotrs1057518071
SNPdbers1057518071
MSV3drs1057518071
GWAS Ctlgrs1057518071
Max Magnitude0
ClinVar
Risk rs1057518071(G;G)
Alt rs1057518071(G;G)
Reference Rs1057518071(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ACTB
CLNDBN not provided
Reversed 1
HGVS NC_000007.13:g.5568098G>C
CLNSRC
CLNACC RCV000414060.1,