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rs768720209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs768720209(A;A)
Make rs768720209(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position126271436
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs768720209
ClinGenrs768720209
ebirs768720209
HLIrs768720209
Exacrs768720209
Varsomers768720209
Maprs768720209
PheGenIrs768720209
hapmaprs768720209
1000 genomesrs768720209
hgdprs768720209
ensemblrs768720209
gopubmedrs768720209
geneviewrs768720209
scholarrs768720209
googlers768720209
pharmgkbrs768720209
gwascentralrs768720209
openSNPrs768720209
23andMers768720209
23andMe allrs768720209
SNP Nexus

SNPshotrs768720209
SNPdbers768720209
MSV3drs768720209
GWAS Ctlgrs768720209
Max Magnitude0
ClinVar
Risk rs768720209(A;A)
Alt rs768720209(A;A)
Reference Rs768720209(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXRED1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.126141331G>A
CLNSRC
CLNACC RCV000196380.1,