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rs1057519152

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519152(A;A)
Make rs1057519152(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position127435360
GeneMEGF10
is asnp
is mentioned by
dbSNPrs1057519152
dbSNP (old)rs1057519152
ClinGenrs1057519152
ebirs1057519152
HLIrs1057519152
Exacrs1057519152
Gnomadrs1057519152
Varsomers1057519152
Maprs1057519152
PheGenIrs1057519152
Biobankrs1057519152
1000 genomesrs1057519152
hgdprs1057519152
ensemblrs1057519152
gopubmedrs1057519152
geneviewrs1057519152
scholarrs1057519152
googlers1057519152
pharmgkbrs1057519152
gwascentralrs1057519152
openSNPrs1057519152
23andMers1057519152
23andMe allrs1057519152
SNPshotrs1057519152
SNPdbers1057519152
MSV3drs1057519152
GWAS Ctlgrs1057519152
Max Magnitude0
ClinVar
Risk rs1057519152(A;A)
Alt rs1057519152(A;A)
Reference Rs1057519152(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MEGF10
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.126771052G>A
CLNSRC
CLNACC RCV000416216.1,