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rs1064793831

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome5
Position127396744
GeneMEGF10
is asnp
is mentioned by
dbSNPrs1064793831
dbSNP (old)rs1064793831
ClinGenrs1064793831
ebirs1064793831
HLIrs1064793831
Exacrs1064793831
Gnomadrs1064793831
Varsomers1064793831
Maprs1064793831
PheGenIrs1064793831
Biobankrs1064793831
1000 genomesrs1064793831
hgdprs1064793831
ensemblrs1064793831
gopubmedrs1064793831
geneviewrs1064793831
scholarrs1064793831
googlers1064793831
pharmgkbrs1064793831
gwascentralrs1064793831
openSNPrs1064793831
23andMers1064793831
23andMe allrs1064793831
SNPshotrs1064793831
SNPdbers1064793831
MSV3drs1064793831
GWAS Ctlgrs1064793831
Max Magnitude0
ClinVar
Risk rs1064793831(T;T)
Alt rs1064793831(T;T)
Reference Rs1064793831(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MEGF10
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.126732436G>T
CLNSRC
CLNACC RCV000479831.1,