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rs886039694

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039694(A;A)
Make rs886039694(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position189052945
GeneCOL5A2
is asnp
is mentioned by
dbSNPrs886039694
dbSNP (classic)rs886039694
ClinGenrs886039694
ebirs886039694
HLIrs886039694
Exacrs886039694
Gnomadrs886039694
Varsomers886039694
LitVarrs886039694
Maprs886039694
PheGenIrs886039694
Biobankrs886039694
1000 genomesrs886039694
hgdprs886039694
ensemblrs886039694
geneviewrs886039694
scholarrs886039694
googlers886039694
pharmgkbrs886039694
gwascentralrs886039694
openSNPrs886039694
23andMers886039694
23andMe allrs886039694
SNPshotrs886039694
SNPdbers886039694
MSV3drs886039694
GWAS Ctlgrs886039694
Max Magnitude0
ClinVar
Risk rs886039694(A;A)
Alt rs886039694(A;A)
Reference Rs886039694(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene COL5A2
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.189917671C>T
CLNSRC
CLNACC RCV000255945.1,