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rs765251030

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs765251030(C;G)
Make rs765251030(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position50582553
GeneCHKB, CHKB-AS1, CHKB-CPT1B
is asnp
is mentioned by
dbSNPrs765251030
dbSNP (classic)rs765251030
ClinGenrs765251030
ebirs765251030
HLIrs765251030
Exacrs765251030
Gnomadrs765251030
Varsomers765251030
LitVarrs765251030
Maprs765251030
PheGenIrs765251030
Biobankrs765251030
1000 genomesrs765251030
hgdprs765251030
ensemblrs765251030
geneviewrs765251030
scholarrs765251030
googlers765251030
pharmgkbrs765251030
gwascentralrs765251030
openSNPrs765251030
23andMers765251030
SNPshotrs765251030
SNPdbers765251030
MSV3drs765251030
GWAS Ctlgrs765251030
Max Magnitude0
ClinVar
Risk rs765251030(G;G)
Alt rs765251030(G;G)
Reference Rs765251030(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene CHKB-AS1 CHKB-CPT1B CHKB
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.51020982C>G
CLNSRC
CLNACC RCV000480811.1,