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rs544236849

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs544236849(C;T)
Make rs544236849(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position126276473
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs544236849
ebirs544236849
HLIrs544236849
Exacrs544236849
Varsomers544236849
Maprs544236849
PheGenIrs544236849
hapmaprs544236849
1000 genomesrs544236849
hgdprs544236849
ensemblrs544236849
gopubmedrs544236849
geneviewrs544236849
scholarrs544236849
googlers544236849
pharmgkbrs544236849
gwascentralrs544236849
openSNPrs544236849
23andMers544236849
23andMe allrs544236849
SNP Nexus

SNPshotrs544236849
SNPdbers544236849
MSV3drs544236849
GWAS Ctlgrs544236849
Max Magnitude0
ClinVar
Risk rs544236849(T;T)
Alt rs544236849(T;T)
Reference rs544236849(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXRED1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.126146368C>T
CLNSRC
CLNACC RCV000199041.2,