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rs747946828

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs747946828(A;A)
Make rs747946828(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position189043231
GeneCOL5A2
is asnp
is mentioned by
dbSNPrs747946828
ebirs747946828
HLIrs747946828
Exacrs747946828
Varsomers747946828
Maprs747946828
PheGenIrs747946828
hapmaprs747946828
1000 genomesrs747946828
hgdprs747946828
ensemblrs747946828
gopubmedrs747946828
geneviewrs747946828
scholarrs747946828
googlers747946828
pharmgkbrs747946828
gwascentralrs747946828
openSNPrs747946828
23andMers747946828
23andMe allrs747946828
SNP Nexus

SNPshotrs747946828
SNPdbers747946828
MSV3drs747946828
GWAS Ctlgrs747946828
Max Magnitude0
ClinVar
Risk rs747946828(A;A)
Alt rs747946828(A;A)
Reference rs747946828(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL5A2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.189907957C>T
CLNSRC
CLNACC RCV000200482.1,