Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057517963

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057517963(A;G)
Make rs1057517963(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome6
Position129502657
GeneLAMA2, LOC102723409
is asnp
is mentioned by
dbSNPrs1057517963
dbSNP (old)rs1057517963
ClinGenrs1057517963
ebirs1057517963
HLIrs1057517963
Exacrs1057517963
Gnomadrs1057517963
Varsomers1057517963
LitVarrs1057517963
Maprs1057517963
PheGenIrs1057517963
Biobankrs1057517963
1000 genomesrs1057517963
hgdprs1057517963
ensemblrs1057517963
gopubmedrs1057517963
geneviewrs1057517963
scholarrs1057517963
googlers1057517963
pharmgkbrs1057517963
gwascentralrs1057517963
openSNPrs1057517963
23andMers1057517963
23andMe allrs1057517963
SNPshotrs1057517963
SNPdbers1057517963
MSV3drs1057517963
GWAS Ctlgrs1057517963
Max Magnitude0
ClinVar
Risk rs1057517963(G;G)
Alt rs1057517963(G;G)
Reference Rs1057517963(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129823802A>G
CLNSRC
CLNACC RCV000414051.1,