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rs1057523896

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523896(A;A)
Make rs1057523896(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position127443046
GeneMEGF10
is asnp
is mentioned by
dbSNPrs1057523896
dbSNP (old)rs1057523896
ClinGenrs1057523896
ebirs1057523896
HLIrs1057523896
Exacrs1057523896
Gnomadrs1057523896
Varsomers1057523896
Maprs1057523896
PheGenIrs1057523896
Biobankrs1057523896
1000 genomesrs1057523896
hgdprs1057523896
ensemblrs1057523896
gopubmedrs1057523896
geneviewrs1057523896
scholarrs1057523896
googlers1057523896
pharmgkbrs1057523896
gwascentralrs1057523896
openSNPrs1057523896
23andMers1057523896
23andMe allrs1057523896
SNPshotrs1057523896
SNPdbers1057523896
MSV3drs1057523896
GWAS Ctlgrs1057523896
Max Magnitude0
ClinVar
Risk rs1057523896(A;A)
Alt rs1057523896(A;A)
Reference Rs1057523896(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEGF10
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.126778738G>A
CLNSRC
CLNACC RCV000418971.1,