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rs1057520739

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520739(C;T)
Make rs1057520739(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position78781863
GeneARSB
is asnp
is mentioned by
dbSNPrs1057520739
dbSNP (old)rs1057520739
ClinGenrs1057520739
ebirs1057520739
HLIrs1057520739
Exacrs1057520739
Gnomadrs1057520739
Varsomers1057520739
Maprs1057520739
PheGenIrs1057520739
Biobankrs1057520739
1000 genomesrs1057520739
hgdprs1057520739
ensemblrs1057520739
gopubmedrs1057520739
geneviewrs1057520739
scholarrs1057520739
googlers1057520739
pharmgkbrs1057520739
gwascentralrs1057520739
openSNPrs1057520739
23andMers1057520739
23andMe allrs1057520739
SNPshotrs1057520739
SNPdbers1057520739
MSV3drs1057520739
GWAS Ctlgrs1057520739
Max Magnitude0
ClinVar
Risk rs1057520739(T;T)
Alt rs1057520739(T;T)
Reference Rs1057520739(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene ARSB
CLNDBN not provided
Reversed 1
HGVS NC_000005.9:g.78077686G>A
CLNSRC
CLNACC RCV000435336.1,