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rs755462817

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755462817(A;A)
Make rs755462817(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position218661852
GeneBCS1L
is asnp
is mentioned by
dbSNPrs755462817
ebirs755462817
HLIrs755462817
Exacrs755462817
Varsomers755462817
Maprs755462817
PheGenIrs755462817
hapmaprs755462817
1000 genomesrs755462817
hgdprs755462817
ensemblrs755462817
gopubmedrs755462817
geneviewrs755462817
scholarrs755462817
googlers755462817
pharmgkbrs755462817
gwascentralrs755462817
openSNPrs755462817
23andMers755462817
23andMe allrs755462817
SNP Nexus

SNPshotrs755462817
SNPdbers755462817
MSV3drs755462817
GWAS Ctlgrs755462817
Max Magnitude0
ClinVar
Risk rs755462817(A;A)
Alt rs755462817(A;A)
Reference rs755462817(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BCS1L
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.219526575G>A
CLNSRC
CLNACC RCV000197835.1,