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rs1064797327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome6
Position129149097
GeneLAMA2
is asnp
is mentioned by
dbSNPrs1064797327
dbSNP (classic)rs1064797327
ClinGenrs1064797327
ebirs1064797327
HLIrs1064797327
Exacrs1064797327
Gnomadrs1064797327
Varsomers1064797327
LitVarrs1064797327
Maprs1064797327
PheGenIrs1064797327
Biobankrs1064797327
1000 genomesrs1064797327
hgdprs1064797327
ensemblrs1064797327
geneviewrs1064797327
scholarrs1064797327
googlers1064797327
pharmgkbrs1064797327
gwascentralrs1064797327
openSNPrs1064797327
23andMers1064797327
SNPshotrs1064797327
SNPdbers1064797327
MSV3drs1064797327
GWAS Ctlgrs1064797327
Max Magnitude0
ClinVar
Risk rs1064797327(A;A)
Alt rs1064797327(A;A)
Reference Rs1064797327(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129470242G>A
CLNSRC
CLNACC RCV000488063.1,