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rs774047700

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs774047700(-;-)
Make rs774047700(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position71553805
GeneDYSF
is asnp
is mentioned by
dbSNPrs774047700
ebirs774047700
HLIrs774047700
Exacrs774047700
Varsomers774047700
Maprs774047700
PheGenIrs774047700
hapmaprs774047700
1000 genomesrs774047700
hgdprs774047700
ensemblrs774047700
gopubmedrs774047700
geneviewrs774047700
scholarrs774047700
googlers774047700
pharmgkbrs774047700
gwascentralrs774047700
openSNPrs774047700
23andMers774047700
23andMe allrs774047700
SNP Nexus

SNPshotrs774047700
SNPdbers774047700
MSV3drs774047700
GWAS Ctlgrs774047700
Max Magnitude0
ClinVar
Risk rs774047700(;)
Alt rs774047700(;)
Reference rs774047700(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.71780935delA
CLNSRC
CLNACC RCV000176197.1,