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rs1085307982

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position110173908
GeneCOL4A1
is asnp
is mentioned by
dbSNPrs1085307982
dbSNP (old)rs1085307982
ClinGenrs1085307982
ebirs1085307982
HLIrs1085307982
Exacrs1085307982
Gnomadrs1085307982
Varsomers1085307982
Maprs1085307982
PheGenIrs1085307982
Biobankrs1085307982
1000 genomesrs1085307982
hgdprs1085307982
ensemblrs1085307982
gopubmedrs1085307982
geneviewrs1085307982
scholarrs1085307982
googlers1085307982
pharmgkbrs1085307982
gwascentralrs1085307982
openSNPrs1085307982
23andMers1085307982
23andMe allrs1085307982
SNPshotrs1085307982
SNPdbers1085307982
MSV3drs1085307982
GWAS Ctlgrs1085307982
Max Magnitude0
ClinVar
Risk rs1085307982(T;T)
Alt rs1085307982(T;T)
Reference Rs1085307982(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A1
CLNDBN not provided
Reversed 1
HGVS NC_000013.10:g.110826255C>A
CLNSRC
CLNACC RCV000489567.1,