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rs786200898

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786200898(-;-)
Make rs786200898(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position71516243
GeneDYSF
is asnp
is mentioned by
dbSNPrs786200898
ebirs786200898
HLIrs786200898
Exacrs786200898
Varsomers786200898
Maprs786200898
PheGenIrs786200898
hapmaprs786200898
1000 genomesrs786200898
hgdprs786200898
ensemblrs786200898
gopubmedrs786200898
geneviewrs786200898
scholarrs786200898
googlers786200898
pharmgkbrs786200898
gwascentralrs786200898
openSNPrs786200898
23andMers786200898
23andMe allrs786200898
SNP Nexus

SNPshotrs786200898
SNPdbers786200898
MSV3drs786200898
GWAS Ctlgrs786200898
Max Magnitude0
ClinVar
Risk rs786200898(;)
Alt rs786200898(;)
Reference rs786200898(G;G)
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.71743373delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007071.4,