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rs786205643

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205643(A;C)
Make rs786205643(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position49132281
GeneLAMB2
is asnp
is mentioned by
dbSNPrs786205643
ebirs786205643
HLIrs786205643
Exacrs786205643
Varsomers786205643
Maprs786205643
PheGenIrs786205643
hapmaprs786205643
1000 genomesrs786205643
hgdprs786205643
ensemblrs786205643
gopubmedrs786205643
geneviewrs786205643
scholarrs786205643
googlers786205643
pharmgkbrs786205643
gwascentralrs786205643
openSNPrs786205643
23andMers786205643
23andMe allrs786205643
SNP Nexus

SNPshotrs786205643
SNPdbers786205643
MSV3drs786205643
GWAS Ctlgrs786205643
Max Magnitude0
ClinVar
Risk rs786205643(C;C)
Alt rs786205643(C;C)
Reference rs786205643(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMB2
CLNDBN not provided
Reversed 1
HGVS NC_000003.11:g.49169714T>G
CLNSRC
CLNACC RCV000171513.1,