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rs886039412

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs886039412(A;A)
Make rs886039412(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome18
Position23928766
GeneLAMA3
is asnp
is mentioned by
dbSNPrs886039412
dbSNP (classic)rs886039412
ClinGenrs886039412
ebirs886039412
HLIrs886039412
Exacrs886039412
Gnomadrs886039412
Varsomers886039412
LitVarrs886039412
Maprs886039412
PheGenIrs886039412
Biobankrs886039412
1000 genomesrs886039412
hgdprs886039412
ensemblrs886039412
geneviewrs886039412
scholarrs886039412
googlers886039412
pharmgkbrs886039412
gwascentralrs886039412
openSNPrs886039412
23andMers886039412
23andMe allrs886039412
SNPshotrs886039412
SNPdbers886039412
MSV3drs886039412
GWAS Ctlgrs886039412
Max Magnitude0
ClinVar
Risk rs886039412(A;A)
Alt rs886039412(A;A)
Reference Rs886039412(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMA3
CLNDBN not provided
Reversed 0
HGVS NC_000018.9:g.21508730G>A
CLNSRC
CLNACC RCV000255139.1,