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rs863223473

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223473(-;C)
Make rs863223473(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134802950
GeneCOL5A1
is asnp
is mentioned by
dbSNPrs863223473
ClinGenrs863223473
ebirs863223473
HLIrs863223473
Exacrs863223473
Varsomers863223473
Maprs863223473
PheGenIrs863223473
hapmaprs863223473
1000 genomesrs863223473
hgdprs863223473
ensemblrs863223473
gopubmedrs863223473
geneviewrs863223473
scholarrs863223473
googlers863223473
pharmgkbrs863223473
gwascentralrs863223473
openSNPrs863223473
23andMers863223473
23andMe allrs863223473
SNP Nexus

SNPshotrs863223473
SNPdbers863223473
MSV3drs863223473
GWAS Ctlgrs863223473
Max Magnitude0
ClinVar
Risk rs863223473(C;C)
Alt rs863223473(C;C)
Reference Rs863223473(;)
Significance Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137694796dupC
CLNSRC
CLNACC RCV000199987.1,