Have questions? Visit https://www.reddit.com/r/SNPedia

rs773209126

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs773209126(C;T)
Make rs773209126(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position129165672
GeneLAMA2
is asnp
is mentioned by
dbSNPrs773209126
ebirs773209126
HLIrs773209126
Exacrs773209126
Varsomers773209126
Maprs773209126
PheGenIrs773209126
hapmaprs773209126
1000 genomesrs773209126
hgdprs773209126
ensemblrs773209126
gopubmedrs773209126
geneviewrs773209126
scholarrs773209126
googlers773209126
pharmgkbrs773209126
gwascentralrs773209126
openSNPrs773209126
23andMers773209126
23andMe allrs773209126
SNP Nexus

SNPshotrs773209126
SNPdbers773209126
MSV3drs773209126
GWAS Ctlgrs773209126
Max Magnitude0
ClinVar
Risk rs773209126(T;T)
Alt rs773209126(T;T)
Reference rs773209126(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129486817C>T
CLNSRC
CLNACC RCV000224579.1,