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rs377464580

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs377464580(A;A)
Make rs377464580(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position126276474
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs377464580
ebirs377464580
HLIrs377464580
Exacrs377464580
Varsomers377464580
Maprs377464580
PheGenIrs377464580
hapmaprs377464580
1000 genomesrs377464580
hgdprs377464580
ensemblrs377464580
gopubmedrs377464580
geneviewrs377464580
scholarrs377464580
googlers377464580
pharmgkbrs377464580
gwascentralrs377464580
openSNPrs377464580
23andMers377464580
23andMe allrs377464580
SNP Nexus

SNPshotrs377464580
SNPdbers377464580
MSV3drs377464580
GWAS Ctlgrs377464580
Max Magnitude0
ClinVar
Risk rs377464580(A;A)
Alt rs377464580(A;A)
Reference rs377464580(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXRED1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.126146369G>A
CLNSRC
CLNACC RCV000195492.1,