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rs200923373

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs200923373(C;T)
Make rs200923373(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome6
Position129342379
GeneLAMA2
is asnp
is mentioned by
dbSNPrs200923373
ebirs200923373
HLIrs200923373
Exacrs200923373
Varsomers200923373
Maprs200923373
PheGenIrs200923373
hapmaprs200923373
1000 genomesrs200923373
hgdprs200923373
ensemblrs200923373
gopubmedrs200923373
geneviewrs200923373
scholarrs200923373
googlers200923373
pharmgkbrs200923373
gwascentralrs200923373
openSNPrs200923373
23andMers200923373
23andMe allrs200923373
SNP Nexus

SNPshotrs200923373
SNPdbers200923373
MSV3drs200923373
GWAS Ctlgrs200923373
Max Magnitude0
ClinVar
Risk rs200923373(T;T)
Alt rs200923373(T;T)
Reference rs200923373(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LAMA2
CLNDBN not provided
Reversed 0
HGVS NC_000006.11:g.129663524C>T
CLNSRC
CLNACC RCV000171401.1,