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rs762065361

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762065361(A;A)
Make rs762065361(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome21
Position43065621
GeneCBS
is asnp
is mentioned by
dbSNPrs762065361
ebirs762065361
HLIrs762065361
Exacrs762065361
Varsomers762065361
Maprs762065361
PheGenIrs762065361
hapmaprs762065361
1000 genomesrs762065361
hgdprs762065361
ensemblrs762065361
gopubmedrs762065361
geneviewrs762065361
scholarrs762065361
googlers762065361
pharmgkbrs762065361
gwascentralrs762065361
openSNPrs762065361
23andMers762065361
23andMe allrs762065361
SNP Nexus

SNPshotrs762065361
SNPdbers762065361
MSV3drs762065361
GWAS Ctlgrs762065361
Max Magnitude0
ClinVar
Risk rs762065361(A;A)
Alt rs762065361(A;A)
Reference rs762065361(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene CBS
CLNDBN not provided
Reversed 0
HGVS NC_000021.8:g.44485731C>A
CLNSRC
CLNACC RCV000200013.1,