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rs10494778

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10494778(A;G)
Make rs10494778(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position198558976
is asnp
is mentioned by
dbSNPrs10494778
dbSNP (classic)rs10494778
ClinGenrs10494778
ebirs10494778
HLIrs10494778
Exacrs10494778
Gnomadrs10494778
Varsomers10494778
LitVarrs10494778
Maprs10494778
PheGenIrs10494778
Biobankrs10494778
1000 genomesrs10494778
hgdprs10494778
ensemblrs10494778
geneviewrs10494778
scholarrs10494778
googlers10494778
pharmgkbrs10494778
gwascentralrs10494778
openSNPrs10494778
23andMers10494778
23andMe allrs10494778
SNPshotrs10494778
SNPdbers10494778
MSV3drs10494778
GWAS Ctlgrs10494778
GMAF0.0955
Max Magnitude0
? (A;A) (A;G) (G;G) 28