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rs748973032

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs748973032(A;A)
Make rs748973032(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50524129
GeneNCAPH2, SCO2
is asnp
is mentioned by
dbSNPrs748973032
ebirs748973032
HLIrs748973032
Exacrs748973032
Varsomers748973032
Maprs748973032
PheGenIrs748973032
hapmaprs748973032
1000 genomesrs748973032
hgdprs748973032
ensemblrs748973032
gopubmedrs748973032
geneviewrs748973032
scholarrs748973032
googlers748973032
pharmgkbrs748973032
gwascentralrs748973032
openSNPrs748973032
23andMers748973032
23andMe allrs748973032
SNP Nexus

SNPshotrs748973032
SNPdbers748973032
MSV3drs748973032
GWAS Ctlgrs748973032
Max Magnitude0
ClinVar
Risk rs748973032(A;A)
Alt rs748973032(A;A)
Reference rs748973032(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NCAPH2 SCO2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.50962558G>A
CLNSRC
CLNACC RCV000196635.1,