Have questions? Visit https://www.reddit.com/r/SNPedia

rs863223915

From SNPedia

Orientationplus
Make rs863223915(-;-)
Make rs863223915(-;AT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position218661923
GeneBCS1L
is asnp
is mentioned by
dbSNPrs863223915
ebirs863223915
HLIrs863223915
Exacrs863223915
Varsomers863223915
Maprs863223915
PheGenIrs863223915
hapmaprs863223915
1000 genomesrs863223915
hgdprs863223915
ensemblrs863223915
gopubmedrs863223915
geneviewrs863223915
scholarrs863223915
googlers863223915
pharmgkbrs863223915
gwascentralrs863223915
openSNPrs863223915
23andMers863223915
23andMe allrs863223915
SNP Nexus

SNPshotrs863223915
SNPdbers863223915
MSV3drs863223915
GWAS Ctlgrs863223915
Max Magnitude
ClinVar
Risk rs863223915(;)
Alt rs863223915(;)
Reference rs863223915(AT;AT)
Significance Pathogenic
Disease not provided
Variation info
Gene BCS1L
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.219526646_219526647delAT
CLNSRC
CLNACC RCV000199046.1,