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rs11557872

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs11557872(C;C)
Make rs11557872(C;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position55234184
GeneCLHC1, RPS27A
is asnp
is mentioned by
dbSNPrs11557872
dbSNP (classic)rs11557872
ClinGenrs11557872
ebirs11557872
HLIrs11557872
Exacrs11557872
Gnomadrs11557872
Varsomers11557872
LitVarrs11557872
Maprs11557872
PheGenIrs11557872
Biobankrs11557872
1000 genomesrs11557872
hgdprs11557872
ensemblrs11557872
geneviewrs11557872
scholarrs11557872
googlers11557872
pharmgkbrs11557872
gwascentralrs11557872
openSNPrs11557872
23andMers11557872
SNPshotrs11557872
SNPdbers11557872
MSV3drs11557872
GWAS Ctlgrs11557872
Max Magnitude0
ClinVar
Risk rs11557872(C;C)
Alt rs11557872(C;C)
Reference Rs11557872(T;T)
Significance Untested
Disease
Variation info
Gene RPS27A CLHC1
CLNDBN
Reversed 0
HGVS NC_000002.11:g.55461320T>C
CLNSRC
CLNACC