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rs863223478

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863223478(C;T)
Make rs863223478(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position134795115
GeneCOL5A1
is asnp
is mentioned by
dbSNPrs863223478
ebirs863223478
HLIrs863223478
Exacrs863223478
Varsomers863223478
Maprs863223478
PheGenIrs863223478
hapmaprs863223478
1000 genomesrs863223478
hgdprs863223478
ensemblrs863223478
gopubmedrs863223478
geneviewrs863223478
scholarrs863223478
googlers863223478
pharmgkbrs863223478
gwascentralrs863223478
openSNPrs863223478
23andMers863223478
23andMe allrs863223478
SNP Nexus

SNPshotrs863223478
SNPdbers863223478
MSV3drs863223478
GWAS Ctlgrs863223478
Max Magnitude0
ClinVar
Risk rs863223478(T;T)
Alt rs863223478(T;T)
Reference rs863223478(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene COL5A1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.137686961C>T
CLNSRC
CLNACC RCV000200816.1,