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rs1057521059

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521059(A;A)
Make rs1057521059(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position218661470
GeneBCS1L, ZNF142
is asnp
is mentioned by
dbSNPrs1057521059
dbSNP (classic)rs1057521059
ClinGenrs1057521059
ebirs1057521059
HLIrs1057521059
Exacrs1057521059
Gnomadrs1057521059
Varsomers1057521059
LitVarrs1057521059
Maprs1057521059
PheGenIrs1057521059
Biobankrs1057521059
1000 genomesrs1057521059
hgdprs1057521059
ensemblrs1057521059
geneviewrs1057521059
scholarrs1057521059
googlers1057521059
pharmgkbrs1057521059
gwascentralrs1057521059
openSNPrs1057521059
23andMers1057521059
23andMe allrs1057521059
SNPshotrs1057521059
SNPdbers1057521059
MSV3drs1057521059
GWAS Ctlgrs1057521059
Max Magnitude0
ClinVar
Risk rs1057521059(A;A)
Alt rs1057521059(A;A)
Reference Rs1057521059(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene ZNF142 BCS1L
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.219526193G>A
CLNSRC
CLNACC RCV000432529.1,