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rs1057520537

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520537(C;T)
Make rs1057520537(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position74461988
GeneMOGS
is asnp
is mentioned by
dbSNPrs1057520537
dbSNP (old)rs1057520537
ClinGenrs1057520537
ebirs1057520537
HLIrs1057520537
Exacrs1057520537
Gnomadrs1057520537
Varsomers1057520537
Maprs1057520537
PheGenIrs1057520537
Biobankrs1057520537
1000 genomesrs1057520537
hgdprs1057520537
ensemblrs1057520537
gopubmedrs1057520537
geneviewrs1057520537
scholarrs1057520537
googlers1057520537
pharmgkbrs1057520537
gwascentralrs1057520537
openSNPrs1057520537
23andMers1057520537
23andMe allrs1057520537
SNPshotrs1057520537
SNPdbers1057520537
MSV3drs1057520537
GWAS Ctlgrs1057520537
Max Magnitude0
ClinVar
Risk rs1057520537(T;T)
Alt rs1057520537(T;T)
Reference Rs1057520537(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MOGS
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.74689115G>A
CLNSRC
CLNACC RCV000444636.1,