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rs117422805

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs117422805(C;T)
Make rs117422805(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position129280072
GeneLAMA2
is asnp
is mentioned by
dbSNPrs117422805
ebirs117422805
HLIrs117422805
Exacrs117422805
Varsomers117422805
Maprs117422805
PheGenIrs117422805
hapmaprs117422805
1000 genomesrs117422805
hgdprs117422805
ensemblrs117422805
gopubmedrs117422805
geneviewrs117422805
scholarrs117422805
googlers117422805
pharmgkbrs117422805
gwascentralrs117422805
openSNPrs117422805
23andMers117422805
23andMe allrs117422805
SNP Nexus

SNPshotrs117422805
SNPdbers117422805
MSV3drs117422805
GWAS Ctlgrs117422805
Max Magnitude0
ClinVar
Risk rs117422805(T;T)
Alt rs117422805(T;T)
Reference rs117422805(C;C)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene LAMA2
CLNDBN not specified
Reversed 0
HGVS NC_000006.11:g.129601217C>T
CLNSRC
CLNACC RCV000149994.2,