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rs1057520747

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520747(A;G)
Make rs1057520747(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position8358249
GeneRERE
is asnp
is mentioned by
dbSNPrs1057520747
dbSNP (old)rs1057520747
ClinGenrs1057520747
ebirs1057520747
HLIrs1057520747
Exacrs1057520747
Gnomadrs1057520747
Varsomers1057520747
Maprs1057520747
PheGenIrs1057520747
Biobankrs1057520747
1000 genomesrs1057520747
hgdprs1057520747
ensemblrs1057520747
gopubmedrs1057520747
geneviewrs1057520747
scholarrs1057520747
googlers1057520747
pharmgkbrs1057520747
gwascentralrs1057520747
openSNPrs1057520747
23andMers1057520747
23andMe allrs1057520747
SNPshotrs1057520747
SNPdbers1057520747
MSV3drs1057520747
GWAS Ctlgrs1057520747
Max Magnitude0
ClinVar
Risk rs1057520747(G;G)
Alt rs1057520747(G;G)
Reference Rs1057520747(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RERE
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.8418309T>C
CLNSRC
CLNACC RCV000441094.1,