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rs780495441

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs780495441(C;T)
Make rs780495441(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189066461
GeneCOL5A2
is asnp
is mentioned by
dbSNPrs780495441
ebirs780495441
HLIrs780495441
Exacrs780495441
Varsomers780495441
Maprs780495441
PheGenIrs780495441
hapmaprs780495441
1000 genomesrs780495441
hgdprs780495441
ensemblrs780495441
gopubmedrs780495441
geneviewrs780495441
scholarrs780495441
googlers780495441
pharmgkbrs780495441
gwascentralrs780495441
openSNPrs780495441
23andMers780495441
23andMe allrs780495441
SNP Nexus

SNPshotrs780495441
SNPdbers780495441
MSV3drs780495441
GWAS Ctlgrs780495441
Max Magnitude0
ClinVar
Risk rs780495441(T;T)
Alt rs780495441(T;T)
Reference rs780495441(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189931187C>T
CLNSRC
CLNACC RCV000198000.1,