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rs1057520772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057520772(A;C)
Make rs1057520772(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome19
Position46756844
GeneFKRP
is asnp
is mentioned by
dbSNPrs1057520772
dbSNP (classic)rs1057520772
ClinGenrs1057520772
ebirs1057520772
HLIrs1057520772
Exacrs1057520772
Gnomadrs1057520772
Varsomers1057520772
LitVarrs1057520772
Maprs1057520772
PheGenIrs1057520772
Biobankrs1057520772
1000 genomesrs1057520772
hgdprs1057520772
ensemblrs1057520772
geneviewrs1057520772
scholarrs1057520772
googlers1057520772
pharmgkbrs1057520772
gwascentralrs1057520772
openSNPrs1057520772
23andMers1057520772
23andMe allrs1057520772
SNPshotrs1057520772
SNPdbers1057520772
MSV3drs1057520772
GWAS Ctlgrs1057520772
Max Magnitude0
ClinVar
Risk rs1057520772(C;C)
Alt rs1057520772(C;C)
Reference Rs1057520772(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FKRP
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.47260101A>C
CLNSRC
CLNACC RCV000436944.1,