Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057524257

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524257(A;A)
Make rs1057524257(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position162318034
GeneGCA, IFIH1
is asnp
is mentioned by
dbSNPrs1057524257
dbSNP (classic)rs1057524257
ClinGenrs1057524257
ebirs1057524257
HLIrs1057524257
Exacrs1057524257
Gnomadrs1057524257
Varsomers1057524257
LitVarrs1057524257
Maprs1057524257
PheGenIrs1057524257
Biobankrs1057524257
1000 genomesrs1057524257
hgdprs1057524257
ensemblrs1057524257
geneviewrs1057524257
scholarrs1057524257
googlers1057524257
pharmgkbrs1057524257
gwascentralrs1057524257
openSNPrs1057524257
23andMers1057524257
SNPshotrs1057524257
SNPdbers1057524257
MSV3drs1057524257
GWAS Ctlgrs1057524257
Max Magnitude0
ClinVar
Risk rs1057524257(A;A)
Alt rs1057524257(A;A)
Reference Rs1057524257(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GCA IFIH1
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.163174544C>T
CLNSRC
CLNACC RCV000439163.1,