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rs200288072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200288072(A;A)
Make rs200288072(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position129050089
GeneLAMA2
is asnp
is mentioned by
dbSNPrs200288072
dbSNP (classic)rs200288072
ClinGenrs200288072
ebirs200288072
HLIrs200288072
Exacrs200288072
Gnomadrs200288072
Varsomers200288072
LitVarrs200288072
Maprs200288072
PheGenIrs200288072
Biobankrs200288072
1000 genomesrs200288072
hgdprs200288072
ensemblrs200288072
geneviewrs200288072
scholarrs200288072
googlers200288072
pharmgkbrs200288072
gwascentralrs200288072
openSNPrs200288072
23andMers200288072
SNPshotrs200288072
SNPdbers200288072
MSV3drs200288072
GWAS Ctlgrs200288072
Max Magnitude0
ClinVar
Risk rs200288072(A;A)
Alt rs200288072(A;A)
Reference Rs200288072(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129371234G>A
CLNSRC
CLNACC RCV000444644.1,