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rs73532636

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs73532636(A;G)
Make rs73532636(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position112139807
GeneLAMA4
is asnp
is mentioned by
dbSNPrs73532636
ebirs73532636
HLIrs73532636
Exacrs73532636
Varsomers73532636
Maprs73532636
PheGenIrs73532636
hapmaprs73532636
1000 genomesrs73532636
hgdprs73532636
ensemblrs73532636
gopubmedrs73532636
geneviewrs73532636
scholarrs73532636
googlers73532636
pharmgkbrs73532636
gwascentralrs73532636
openSNPrs73532636
23andMers73532636
23andMe allrs73532636
SNP Nexus

SNPshotrs73532636
SNPdbers73532636
MSV3drs73532636
GWAS Ctlgrs73532636
Max Magnitude0
ClinVar
Risk rs73532636(G;G)
Alt rs73532636(G;G)
Reference rs73532636(A;A)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene LAMA4
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.112461009A>G
CLNSRC
CLNACC RCV000200106.2,