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rs863223448

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223448(C;C)
Make rs863223448(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134806280
GeneCOL5A1
is asnp
is mentioned by
dbSNPrs863223448
ebirs863223448
HLIrs863223448
Exacrs863223448
Varsomers863223448
Maprs863223448
PheGenIrs863223448
hapmaprs863223448
1000 genomesrs863223448
hgdprs863223448
ensemblrs863223448
gopubmedrs863223448
geneviewrs863223448
scholarrs863223448
googlers863223448
pharmgkbrs863223448
gwascentralrs863223448
openSNPrs863223448
23andMers863223448
23andMe allrs863223448
SNP Nexus

SNPshotrs863223448
SNPdbers863223448
MSV3drs863223448
GWAS Ctlgrs863223448
Max Magnitude0
ClinVar
Risk rs863223448(C;C)
Alt rs863223448(C;C)
Reference rs863223448(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137698126G>C
CLNSRC
CLNACC RCV000196835.2,