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rs1064794941

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome6
Position129190236
GeneLAMA2
is asnp
is mentioned by
dbSNPrs1064794941
dbSNP (old)rs1064794941
ClinGenrs1064794941
ebirs1064794941
HLIrs1064794941
Exacrs1064794941
Gnomadrs1064794941
Varsomers1064794941
Maprs1064794941
PheGenIrs1064794941
Biobankrs1064794941
1000 genomesrs1064794941
hgdprs1064794941
ensemblrs1064794941
gopubmedrs1064794941
geneviewrs1064794941
scholarrs1064794941
googlers1064794941
pharmgkbrs1064794941
gwascentralrs1064794941
openSNPrs1064794941
23andMers1064794941
23andMe allrs1064794941
SNPshotrs1064794941
SNPdbers1064794941
MSV3drs1064794941
GWAS Ctlgrs1064794941
Max Magnitude0
ClinVar
Risk rs1064794941(A;A)
Alt rs1064794941(A;A)
Reference Rs1064794941(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129511381G>A
CLNSRC
CLNACC RCV000484636.1,