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rs1057518119

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057518119(A;A)
Make rs1057518119(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position129314799
GeneLAMA2
is asnp
is mentioned by
dbSNPrs1057518119
dbSNP (classic)rs1057518119
ClinGenrs1057518119
ebirs1057518119
HLIrs1057518119
Exacrs1057518119
Gnomadrs1057518119
Varsomers1057518119
LitVarrs1057518119
Maprs1057518119
PheGenIrs1057518119
Biobankrs1057518119
1000 genomesrs1057518119
hgdprs1057518119
ensemblrs1057518119
geneviewrs1057518119
scholarrs1057518119
googlers1057518119
pharmgkbrs1057518119
gwascentralrs1057518119
openSNPrs1057518119
23andMers1057518119
23andMe allrs1057518119
SNPshotrs1057518119
SNPdbers1057518119
MSV3drs1057518119
GWAS Ctlgrs1057518119
Max Magnitude0
ClinVar
Risk rs1057518119(A;A)
Alt rs1057518119(A;A)
Reference Rs1057518119(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129635944G>A
CLNSRC
CLNACC RCV000413320.1,