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rs1085307983

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome13
Position110491286
GeneCOL4A2
is asnp
is mentioned by
dbSNPrs1085307983
dbSNP (old)rs1085307983
ClinGenrs1085307983
ebirs1085307983
HLIrs1085307983
Exacrs1085307983
Gnomadrs1085307983
Varsomers1085307983
Maprs1085307983
PheGenIrs1085307983
Biobankrs1085307983
1000 genomesrs1085307983
hgdprs1085307983
ensemblrs1085307983
gopubmedrs1085307983
geneviewrs1085307983
scholarrs1085307983
googlers1085307983
pharmgkbrs1085307983
gwascentralrs1085307983
openSNPrs1085307983
23andMers1085307983
23andMe allrs1085307983
SNPshotrs1085307983
SNPdbers1085307983
MSV3drs1085307983
GWAS Ctlgrs1085307983
Max Magnitude0
ClinVar
Risk rs1085307983(A;A)
Alt rs1085307983(A;A)
Reference Rs1085307983(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene COL4A2
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.111143633G>A
CLNSRC
CLNACC RCV000490216.1,