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rs780314255

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs780314255(A;A)
Make rs780314255(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position50523877
GeneNCAPH2, SCO2
is asnp
is mentioned by
dbSNPrs780314255
ebirs780314255
HLIrs780314255
Exacrs780314255
Varsomers780314255
Maprs780314255
PheGenIrs780314255
hapmaprs780314255
1000 genomesrs780314255
hgdprs780314255
ensemblrs780314255
gopubmedrs780314255
geneviewrs780314255
scholarrs780314255
googlers780314255
pharmgkbrs780314255
gwascentralrs780314255
openSNPrs780314255
23andMers780314255
23andMe allrs780314255
SNP Nexus

SNPshotrs780314255
SNPdbers780314255
MSV3drs780314255
GWAS Ctlgrs780314255
Max Magnitude0
ClinVar
Risk rs780314255(A;A)
Alt rs780314255(A;A)
Reference rs780314255(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCO2 NCAPH2
CLNDBN not provided
Reversed 0
HGVS NC_000022.10:g.50962306G>A
CLNSRC
CLNACC RCV000197926.1,