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rs769250383

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs769250383(A;G)
Make rs769250383(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50523705
GeneNCAPH2, SCO2
is asnp
is mentioned by
dbSNPrs769250383
ebirs769250383
HLIrs769250383
Exacrs769250383
Varsomers769250383
Maprs769250383
PheGenIrs769250383
hapmaprs769250383
1000 genomesrs769250383
hgdprs769250383
ensemblrs769250383
gopubmedrs769250383
geneviewrs769250383
scholarrs769250383
googlers769250383
pharmgkbrs769250383
gwascentralrs769250383
openSNPrs769250383
23andMers769250383
23andMe allrs769250383
SNP Nexus

SNPshotrs769250383
SNPdbers769250383
MSV3drs769250383
GWAS Ctlgrs769250383
Max Magnitude0
ClinVar
Risk rs769250383(G;G)
Alt rs769250383(G;G)
Reference rs769250383(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCO2 NCAPH2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.50962134A>G
CLNSRC
CLNACC RCV000199522.1,