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rs201495678

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs201495678(A;A)
Make rs201495678(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position162310882
GeneIFIH1
is asnp
is mentioned by
dbSNPrs201495678
dbSNP (old)rs201495678
ClinGenrs201495678
ebirs201495678
HLIrs201495678
Exacrs201495678
Gnomadrs201495678
Varsomers201495678
LitVarrs201495678
Maprs201495678
PheGenIrs201495678
Biobankrs201495678
1000 genomesrs201495678
hgdprs201495678
ensemblrs201495678
gopubmedrs201495678
geneviewrs201495678
scholarrs201495678
googlers201495678
pharmgkbrs201495678
gwascentralrs201495678
openSNPrs201495678
23andMers201495678
23andMe allrs201495678
SNPshotrs201495678
SNPdbers201495678
MSV3drs201495678
GWAS Ctlgrs201495678
Max Magnitude0
ClinVar
Risk rs201495678(A;A)
Alt rs201495678(A;A)
Reference Rs201495678(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene IFIH1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.163167392T>A
CLNSRC
CLNACC RCV000488289.1,