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rs35297901

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs35297901(A;A)
Make rs35297901(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position71564125
GeneDYSF
is asnp
is mentioned by
dbSNPrs35297901
dbSNP (classic)rs35297901
ClinGenrs35297901
ebirs35297901
HLIrs35297901
Exacrs35297901
Gnomadrs35297901
Varsomers35297901
LitVarrs35297901
Maprs35297901
PheGenIrs35297901
Biobankrs35297901
1000 genomesrs35297901
hgdprs35297901
ensemblrs35297901
geneviewrs35297901
scholarrs35297901
googlers35297901
pharmgkbrs35297901
gwascentralrs35297901
openSNPrs35297901
23andMers35297901
23andMe allrs35297901
SNPshotrs35297901
SNPdbers35297901
MSV3drs35297901
GWAS Ctlgrs35297901
Max Magnitude0


ClinVar
Risk rs35297901(A;A)
Alt rs35297901(A;A)
Reference Rs35297901(G;G)
Significance Unknown
Disease Miyoshi myopathy not specified Limb-Girdle Muscular Dystrophy
Variation info
Gene DYSF
CLNDBN Miyoshi myopathy not specified Limb-Girdle Muscular Dystrophy, Recessive
Reversed 0
HGVS NC_000002.11:g.71791255G>A
CLNSRC
CLNACC RCV000271598.1, RCV000356959.2, RCV000366269.1,