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rs1064796486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position218662628
GeneBCS1L
is asnp
is mentioned by
dbSNPrs1064796486
dbSNP (old)rs1064796486
ClinGenrs1064796486
ebirs1064796486
HLIrs1064796486
Exacrs1064796486
Gnomadrs1064796486
Varsomers1064796486
Maprs1064796486
PheGenIrs1064796486
Biobankrs1064796486
1000 genomesrs1064796486
hgdprs1064796486
ensemblrs1064796486
gopubmedrs1064796486
geneviewrs1064796486
scholarrs1064796486
googlers1064796486
pharmgkbrs1064796486
gwascentralrs1064796486
openSNPrs1064796486
23andMers1064796486
23andMe allrs1064796486
SNPshotrs1064796486
SNPdbers1064796486
MSV3drs1064796486
GWAS Ctlgrs1064796486
Max Magnitude0
ClinVar
Risk rs1064796486(T;T)
Alt rs1064796486(T;T)
Reference Rs1064796486(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene BCS1L
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.219527351C>T
CLNSRC
CLNACC RCV000480400.1,