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

rs766920075

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs766920075(C;T)
Make rs766920075(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position129486534
GeneLAMA2
is asnp
is mentioned by
dbSNPrs766920075
ebirs766920075
HLIrs766920075
Exacrs766920075
Varsomers766920075
Maprs766920075
PheGenIrs766920075
hapmaprs766920075
1000 genomesrs766920075
hgdprs766920075
ensemblrs766920075
gopubmedrs766920075
geneviewrs766920075
scholarrs766920075
googlers766920075
pharmgkbrs766920075
gwascentralrs766920075
openSNPrs766920075
23andMers766920075
23andMe allrs766920075
SNP Nexus

SNPshotrs766920075
SNPdbers766920075
MSV3drs766920075
GWAS Ctlgrs766920075
Max Magnitude0
ClinVar
Risk rs766920075(T;T)
Alt rs766920075(T;T)
Reference rs766920075(C;C)
Significance Pathogenic
Disease Merosin deficient congenital muscular dystrophy
Variation info
Gene LAMA2
CLNDBN Merosin deficient congenital muscular dystrophy
Reversed 0
HGVS NC_000006.11:g.129807679C>T
CLNSRC
CLNACC RCV000179173.1,