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rs1064795464

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome18
Position7015724
GeneLAMA1
is asnp
is mentioned by
dbSNPrs1064795464
dbSNP (old)rs1064795464
ClinGenrs1064795464
ebirs1064795464
HLIrs1064795464
Exacrs1064795464
Gnomadrs1064795464
Varsomers1064795464
Maprs1064795464
PheGenIrs1064795464
Biobankrs1064795464
1000 genomesrs1064795464
hgdprs1064795464
ensemblrs1064795464
gopubmedrs1064795464
geneviewrs1064795464
scholarrs1064795464
googlers1064795464
pharmgkbrs1064795464
gwascentralrs1064795464
openSNPrs1064795464
23andMers1064795464
23andMe allrs1064795464
SNPshotrs1064795464
SNPdbers1064795464
MSV3drs1064795464
GWAS Ctlgrs1064795464
Max Magnitude0
ClinVar
Risk rs1064795464(T;T)
Alt rs1064795464(T;T)
Reference Rs1064795464(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA1
CLNDBN not provided
Reversed 1
HGVS NC_000018.9:g.7015723G>A
CLNSRC
CLNACC RCV000486176.1,