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rs1057517756

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517756(C;T)
Make rs1057517756(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome18
Position7049182
GeneLAMA1
is asnp
is mentioned by
dbSNPrs1057517756
dbSNP (old)rs1057517756
ClinGenrs1057517756
ebirs1057517756
HLIrs1057517756
Exacrs1057517756
Gnomadrs1057517756
Varsomers1057517756
Maprs1057517756
PheGenIrs1057517756
Biobankrs1057517756
1000 genomesrs1057517756
hgdprs1057517756
ensemblrs1057517756
gopubmedrs1057517756
geneviewrs1057517756
scholarrs1057517756
googlers1057517756
pharmgkbrs1057517756
gwascentralrs1057517756
openSNPrs1057517756
23andMers1057517756
23andMe allrs1057517756
SNPshotrs1057517756
SNPdbers1057517756
MSV3drs1057517756
GWAS Ctlgrs1057517756
Max Magnitude0
ClinVar
Risk rs1057517756(T;T)
Alt rs1057517756(T;T)
Reference Rs1057517756(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA1
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.7049181G>A
CLNSRC
CLNACC RCV000414527.1,