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rs863223495

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223495(G;T)
Make rs863223495(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189043203
GeneCOL5A2
is asnp
is mentioned by
dbSNPrs863223495
ebirs863223495
HLIrs863223495
Exacrs863223495
Varsomers863223495
Maprs863223495
PheGenIrs863223495
hapmaprs863223495
1000 genomesrs863223495
hgdprs863223495
ensemblrs863223495
gopubmedrs863223495
geneviewrs863223495
scholarrs863223495
googlers863223495
pharmgkbrs863223495
gwascentralrs863223495
openSNPrs863223495
23andMers863223495
23andMe allrs863223495
SNP Nexus

SNPshotrs863223495
SNPdbers863223495
MSV3drs863223495
GWAS Ctlgrs863223495
Max Magnitude0
ClinVar
Risk rs863223495(T;T)
Alt rs863223495(T;T)
Reference rs863223495(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.189907929C>A
CLNSRC
CLNACC RCV000198760.1,