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rs863223723

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223723(A;A)
Make rs863223723(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position2229112
GeneSKI
is asnp
is mentioned by
dbSNPrs863223723
ebirs863223723
HLIrs863223723
Exacrs863223723
Varsomers863223723
Maprs863223723
PheGenIrs863223723
hapmaprs863223723
1000 genomesrs863223723
hgdprs863223723
ensemblrs863223723
gopubmedrs863223723
geneviewrs863223723
scholarrs863223723
googlers863223723
pharmgkbrs863223723
gwascentralrs863223723
openSNPrs863223723
23andMers863223723
23andMe allrs863223723
SNP Nexus

SNPshotrs863223723
SNPdbers863223723
MSV3drs863223723
GWAS Ctlgrs863223723
Max Magnitude0
ClinVar
Risk rs863223723(A;A)
Alt rs863223723(A;A)
Reference rs863223723(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SKI
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.2160551G>A
CLNSRC
CLNACC RCV000198814.1,