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rs863223483

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863223483(G;G)
Make rs863223483(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134842272
GeneCOL5A1, LOC101448202
is asnp
is mentioned by
dbSNPrs863223483
ebirs863223483
HLIrs863223483
Exacrs863223483
Varsomers863223483
Maprs863223483
PheGenIrs863223483
hapmaprs863223483
1000 genomesrs863223483
hgdprs863223483
ensemblrs863223483
gopubmedrs863223483
geneviewrs863223483
scholarrs863223483
googlers863223483
pharmgkbrs863223483
gwascentralrs863223483
openSNPrs863223483
23andMers863223483
23andMe allrs863223483
SNP Nexus

SNPshotrs863223483
SNPdbers863223483
MSV3drs863223483
GWAS Ctlgrs863223483
Max Magnitude0
ClinVar
Risk rs863223483(G;G)
Alt rs863223483(G;G)
Reference rs863223483(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137734118T>G
CLNSRC
CLNACC RCV000195957.1,