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rs786205654

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205654(-;-)
Make rs786205654(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position129192832
GeneLAMA2
is asnp
is mentioned by
dbSNPrs786205654
ebirs786205654
HLIrs786205654
Exacrs786205654
Varsomers786205654
Maprs786205654
PheGenIrs786205654
hapmaprs786205654
1000 genomesrs786205654
hgdprs786205654
ensemblrs786205654
gopubmedrs786205654
geneviewrs786205654
scholarrs786205654
googlers786205654
pharmgkbrs786205654
gwascentralrs786205654
openSNPrs786205654
23andMers786205654
23andMe allrs786205654
SNP Nexus

SNPshotrs786205654
SNPdbers786205654
MSV3drs786205654
GWAS Ctlgrs786205654
Max Magnitude0
ClinVar
Risk rs786205654(;)
Alt rs786205654(;)
Reference rs786205654(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129513977delG
CLNSRC
CLNACC RCV000171527.1,