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rs863223541

From SNPedia

Orientationminus
Make rs863223541(-;-)
Make rs863223541(-;TG)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position127818255
GeneENG
is asnp
is mentioned by
dbSNPrs863223541
ebirs863223541
HLIrs863223541
Exacrs863223541
Varsomers863223541
Maprs863223541
PheGenIrs863223541
hapmaprs863223541
1000 genomesrs863223541
hgdprs863223541
ensemblrs863223541
gopubmedrs863223541
geneviewrs863223541
scholarrs863223541
googlers863223541
pharmgkbrs863223541
gwascentralrs863223541
openSNPrs863223541
23andMers863223541
23andMe allrs863223541
SNP Nexus

SNPshotrs863223541
SNPdbers863223541
MSV3drs863223541
GWAS Ctlgrs863223541
Max Magnitude
ClinVar
Risk rs863223541(;)
Alt rs863223541(;)
Reference rs863223541(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene ENG
CLNDBN not provided
Reversed 1
HGVS NC_000009.11:g.130580534_130580535delCA
CLNSRC
CLNACC RCV000197179.1,