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rs863223690

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223690(A;A)
Make rs863223690(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position112191734
GeneLAMA4
is asnp
is mentioned by
dbSNPrs863223690
ebirs863223690
HLIrs863223690
Exacrs863223690
Varsomers863223690
Maprs863223690
PheGenIrs863223690
hapmaprs863223690
1000 genomesrs863223690
hgdprs863223690
ensemblrs863223690
gopubmedrs863223690
geneviewrs863223690
scholarrs863223690
googlers863223690
pharmgkbrs863223690
gwascentralrs863223690
openSNPrs863223690
23andMers863223690
23andMe allrs863223690
SNP Nexus

SNPshotrs863223690
SNPdbers863223690
MSV3drs863223690
GWAS Ctlgrs863223690
Max Magnitude0
ClinVar
Risk rs863223690(A;A)
Alt rs863223690(A;A)
Reference rs863223690(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA4
CLNDBN not provided
Reversed 1
HGVS NC_000006.11:g.112512936C>T
CLNSRC
CLNACC RCV000197110.1,