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rs1057524616

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524616(G;T)
Make rs1057524616(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position129342472
GeneLAMA2
is asnp
is mentioned by
dbSNPrs1057524616
dbSNP (old)rs1057524616
ClinGenrs1057524616
ebirs1057524616
HLIrs1057524616
Exacrs1057524616
Gnomadrs1057524616
Varsomers1057524616
LitVarrs1057524616
Maprs1057524616
PheGenIrs1057524616
Biobankrs1057524616
1000 genomesrs1057524616
hgdprs1057524616
ensemblrs1057524616
gopubmedrs1057524616
geneviewrs1057524616
scholarrs1057524616
googlers1057524616
pharmgkbrs1057524616
gwascentralrs1057524616
openSNPrs1057524616
23andMers1057524616
23andMe allrs1057524616
SNPshotrs1057524616
SNPdbers1057524616
MSV3drs1057524616
GWAS Ctlgrs1057524616
Max Magnitude0
ClinVar
Risk rs1057524616(T;T)
Alt rs1057524616(T;T)
Reference Rs1057524616(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129663617G>T
CLNSRC
CLNACC RCV000424965.1,