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rs1064795948

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome5
Position127443042
GeneMEGF10
is asnp
is mentioned by
dbSNPrs1064795948
dbSNP (classic)rs1064795948
ClinGenrs1064795948
ebirs1064795948
HLIrs1064795948
Exacrs1064795948
Gnomadrs1064795948
Varsomers1064795948
LitVarrs1064795948
Maprs1064795948
PheGenIrs1064795948
Biobankrs1064795948
1000 genomesrs1064795948
hgdprs1064795948
ensemblrs1064795948
geneviewrs1064795948
scholarrs1064795948
googlers1064795948
pharmgkbrs1064795948
gwascentralrs1064795948
openSNPrs1064795948
23andMers1064795948
23andMe allrs1064795948
SNPshotrs1064795948
SNPdbers1064795948
MSV3drs1064795948
GWAS Ctlgrs1064795948
Max Magnitude0
ClinVar
Risk rs1064795948(-;-)
Alt rs1064795948(-;-)
Reference Rs1064795948(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEGF10
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.126778734delG
CLNSRC
CLNACC RCV000480679.1,