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rs773726323

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773726323(C;T)
Make rs773726323(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189062882
GeneCOL5A2
is asnp
is mentioned by
dbSNPrs773726323
ebirs773726323
HLIrs773726323
Exacrs773726323
Varsomers773726323
Maprs773726323
PheGenIrs773726323
hapmaprs773726323
1000 genomesrs773726323
hgdprs773726323
ensemblrs773726323
gopubmedrs773726323
geneviewrs773726323
scholarrs773726323
googlers773726323
pharmgkbrs773726323
gwascentralrs773726323
openSNPrs773726323
23andMers773726323
23andMe allrs773726323
SNP Nexus

SNPshotrs773726323
SNPdbers773726323
MSV3drs773726323
GWAS Ctlgrs773726323
Max Magnitude0
ClinVar
Risk rs773726323(T;T)
Alt rs773726323(T;T)
Reference rs773726323(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene COL5A2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189927608C>T
CLNSRC
CLNACC RCV000200772.1,