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rs748859459

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748859459(C;T)
Make rs748859459(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position218661851
GeneBCS1L
is asnp
is mentioned by
dbSNPrs748859459
ebirs748859459
HLIrs748859459
Exacrs748859459
Varsomers748859459
Maprs748859459
PheGenIrs748859459
hapmaprs748859459
1000 genomesrs748859459
hgdprs748859459
ensemblrs748859459
gopubmedrs748859459
geneviewrs748859459
scholarrs748859459
googlers748859459
pharmgkbrs748859459
gwascentralrs748859459
openSNPrs748859459
23andMers748859459
23andMe allrs748859459
SNP Nexus

SNPshotrs748859459
SNPdbers748859459
MSV3drs748859459
GWAS Ctlgrs748859459
Max Magnitude0
ClinVar
Risk rs748859459(T;T)
Alt rs748859459(T;T)
Reference rs748859459(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene BCS1L
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.219526574C>T
CLNSRC
CLNACC RCV000196315.2,