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rs1085307994

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome1
Position209629742
GeneLAMB3
is asnp
is mentioned by
dbSNPrs1085307994
dbSNP (old)rs1085307994
ClinGenrs1085307994
ebirs1085307994
HLIrs1085307994
Exacrs1085307994
Gnomadrs1085307994
Varsomers1085307994
Maprs1085307994
PheGenIrs1085307994
Biobankrs1085307994
1000 genomesrs1085307994
hgdprs1085307994
ensemblrs1085307994
gopubmedrs1085307994
geneviewrs1085307994
scholarrs1085307994
googlers1085307994
pharmgkbrs1085307994
gwascentralrs1085307994
openSNPrs1085307994
23andMers1085307994
23andMe allrs1085307994
SNPshotrs1085307994
SNPdbers1085307994
MSV3drs1085307994
GWAS Ctlgrs1085307994
Max Magnitude0
ClinVar
Risk rs1085307994(C;C)
Alt rs1085307994(C;C)
Reference Rs1085307994(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMB3
CLNDBN not provided
Reversed 1
HGVS NC_000001.10:g.209803087C>G
CLNSRC
CLNACC RCV000490089.1,