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rs786205520

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205520(C;C)
Make rs786205520(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position46755483
GeneFKRP
is asnp
is mentioned by
dbSNPrs786205520
ebirs786205520
HLIrs786205520
Exacrs786205520
Varsomers786205520
Maprs786205520
PheGenIrs786205520
hapmaprs786205520
1000 genomesrs786205520
hgdprs786205520
ensemblrs786205520
gopubmedrs786205520
geneviewrs786205520
scholarrs786205520
googlers786205520
pharmgkbrs786205520
gwascentralrs786205520
openSNPrs786205520
23andMers786205520
23andMe allrs786205520
SNP Nexus

SNPshotrs786205520
SNPdbers786205520
MSV3drs786205520
GWAS Ctlgrs786205520
Max Magnitude0
ClinVar
Risk rs786205520(C;C)
Alt rs786205520(C;C)
Reference rs786205520(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FKRP
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.47258740G>C
CLNSRC
CLNACC RCV000171285.1,