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rs797044758

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797044758(-;A)
Make rs797044758(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156135262
GeneLMNA
is asnp
is mentioned by
dbSNPrs797044758
ClinGenrs797044758
ebirs797044758
HLIrs797044758
Exacrs797044758
Varsomers797044758
Maprs797044758
PheGenIrs797044758
hapmaprs797044758
1000 genomesrs797044758
hgdprs797044758
ensemblrs797044758
gopubmedrs797044758
geneviewrs797044758
scholarrs797044758
googlers797044758
pharmgkbrs797044758
gwascentralrs797044758
openSNPrs797044758
23andMers797044758
23andMe allrs797044758
SNP Nexus

SNPshotrs797044758
SNPdbers797044758
MSV3drs797044758
GWAS Ctlgrs797044758
Max Magnitude0
ClinVar
Risk rs797044758(A;A)
Alt rs797044758(A;A)
Reference Rs797044758(-;-)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene LMNA
CLNDBN Limb-girdle muscular dystrophy, type 1B
Reversed 0
HGVS NC_000001.10:g.156105053_156105054insA
CLNSRC
CLNACC RCV000178907.1,