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rs863224105

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224105(A;A)
Make rs863224105(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position161213661
GeneFCER1G, NDUFS2
is asnp
is mentioned by
dbSNPrs863224105
ebirs863224105
HLIrs863224105
Exacrs863224105
Varsomers863224105
Maprs863224105
PheGenIrs863224105
hapmaprs863224105
1000 genomesrs863224105
hgdprs863224105
ensemblrs863224105
gopubmedrs863224105
geneviewrs863224105
scholarrs863224105
googlers863224105
pharmgkbrs863224105
gwascentralrs863224105
openSNPrs863224105
23andMers863224105
23andMe allrs863224105
SNP Nexus

SNPshotrs863224105
SNPdbers863224105
MSV3drs863224105
GWAS Ctlgrs863224105
Max Magnitude0
ClinVar
Risk rs863224105(A;A)
Alt rs863224105(A;A)
Reference rs863224105(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS2 FCER1G
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.161183451G>A
CLNSRC
CLNACC RCV000195512.1,