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rs370874727

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs370874727(A;G)
Make rs370874727(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position71589591
GeneDYSF
is asnp
is mentioned by
dbSNPrs370874727
ebirs370874727
HLIrs370874727
Exacrs370874727
Varsomers370874727
Maprs370874727
PheGenIrs370874727
hapmaprs370874727
1000 genomesrs370874727
hgdprs370874727
ensemblrs370874727
gopubmedrs370874727
geneviewrs370874727
scholarrs370874727
googlers370874727
pharmgkbrs370874727
gwascentralrs370874727
openSNPrs370874727
23andMers370874727
23andMe allrs370874727
SNP Nexus

SNPshotrs370874727
SNPdbers370874727
MSV3drs370874727
GWAS Ctlgrs370874727
Max Magnitude0
ClinVar
Risk rs370874727(G;G)
Alt rs370874727(G;G)
Reference rs370874727(A;A)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene DYSF
CLNDBN Limb-girdle muscular dystrophy, type 2B
Reversed 0
HGVS NC_000002.11:g.71816721A>G
CLNSRC
CLNACC RCV000177553.1,