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rs587777927

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587777927(-;-)
Make rs587777927(-;T)
Make rs587777927(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position117652853
GeneCFTR
is asnp
is mentioned by
dbSNPrs587777927
ebirs587777927
HLIrs587777927
Exacrs587777927
Varsomers587777927
Maprs587777927
PheGenIrs587777927
hapmaprs587777927
1000 genomesrs587777927
hgdprs587777927
ensemblrs587777927
gopubmedrs587777927
geneviewrs587777927
scholarrs587777927
googlers587777927
pharmgkbrs587777927
gwascentralrs587777927
openSNPrs587777927
23andMers587777927
23andMe allrs587777927
SNP Nexus

SNPshotrs587777927
SNPdbers587777927
MSV3drs587777927
GWAS Ctlgrs587777927
Max Magnitude0
ClinVar
Risk rs587777927(T;T)
Alt rs587777927(T;T)
Reference rs587777927(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117292911dupT
CLNSRC CFTR2
CLNACC RCV000047018.4,