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rs200679026

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs200679026(A;A)
Make rs200679026(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position94605552
GeneFBP1
is asnp
is mentioned by
dbSNPrs200679026
ebirs200679026
HLIrs200679026
Exacrs200679026
Varsomers200679026
Maprs200679026
PheGenIrs200679026
hapmaprs200679026
1000 genomesrs200679026
hgdprs200679026
ensemblrs200679026
gopubmedrs200679026
geneviewrs200679026
scholarrs200679026
googlers200679026
pharmgkbrs200679026
gwascentralrs200679026
openSNPrs200679026
23andMers200679026
23andMe allrs200679026
SNP Nexus

SNPshotrs200679026
SNPdbers200679026
MSV3drs200679026
GWAS Ctlgrs200679026
Max Magnitude0
ClinVar
Risk rs200679026(A;A)
Alt rs200679026(A;A)
Reference rs200679026(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FBP1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.97367834G>A
CLNSRC
CLNACC RCV000197614.1,