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rs878853066

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853066(A;G)
Make rs878853066(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position162281524
GeneIFIH1
is asnp
is mentioned by
dbSNPrs878853066
ebirs878853066
HLIrs878853066
Exacrs878853066
Varsomers878853066
Maprs878853066
PheGenIrs878853066
hapmaprs878853066
1000 genomesrs878853066
hgdprs878853066
ensemblrs878853066
gopubmedrs878853066
geneviewrs878853066
scholarrs878853066
googlers878853066
pharmgkbrs878853066
gwascentralrs878853066
openSNPrs878853066
23andMers878853066
23andMe allrs878853066
SNP Nexus

SNPshotrs878853066
SNPdbers878853066
MSV3drs878853066
GWAS Ctlgrs878853066
Max Magnitude0
ClinVar
Risk rs878853066(G;G)
Alt rs878853066(G;G)
Reference rs878853066(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene IFIH1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.163138034T>C
CLNSRC
CLNACC RCV000224540.1,