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rs587777926

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777926(-;-)
Make rs587777926(-;A)
Make rs587777926(A;A)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position117542027
GeneCFTR
is asnp
is mentioned by
dbSNPrs587777926
ebirs587777926
HLIrs587777926
Exacrs587777926
Varsomers587777926
Maprs587777926
PheGenIrs587777926
hapmaprs587777926
1000 genomesrs587777926
hgdprs587777926
ensemblrs587777926
gopubmedrs587777926
geneviewrs587777926
scholarrs587777926
googlers587777926
pharmgkbrs587777926
gwascentralrs587777926
openSNPrs587777926
23andMers587777926
23andMe allrs587777926
SNP Nexus

SNPshotrs587777926
SNPdbers587777926
MSV3drs587777926
GWAS Ctlgrs587777926
Max Magnitude0
ClinVar
Risk rs587777926(A;A)
Alt rs587777926(A;A)
Reference rs587777926(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182081dupA
CLNSRC CFTR2
CLNACC RCV000056341.3,