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rs1064797328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACTG;ACTG) 0 common in clinvar
Chromosome6
Position129460317
GeneLAMA2
is asnp
is mentioned by
dbSNPrs1064797328
dbSNP (classic)rs1064797328
ClinGenrs1064797328
ebirs1064797328
HLIrs1064797328
Exacrs1064797328
Gnomadrs1064797328
Varsomers1064797328
LitVarrs1064797328
Maprs1064797328
PheGenIrs1064797328
Biobankrs1064797328
1000 genomesrs1064797328
hgdprs1064797328
ensemblrs1064797328
geneviewrs1064797328
scholarrs1064797328
googlers1064797328
pharmgkbrs1064797328
gwascentralrs1064797328
openSNPrs1064797328
23andMers1064797328
23andMe allrs1064797328
SNPshotrs1064797328
SNPdbers1064797328
MSV3drs1064797328
GWAS Ctlgrs1064797328
Max Magnitude0
ClinVar
Risk rs1064797328(-;-)
Alt rs1064797328(-;-)
Reference Rs1064797328(ACTG;ACTG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129781462_129781465delACTG
CLNSRC
CLNACC RCV000488369.1,