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rs773569201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T)
(T;T) 0 common/normal


Make rs773569201(A;A)
ReferenceGRCh38.p7 38.3/151
Chromosome7
Position117590397
GeneCFTR
is asnp
is mentioned by
dbSNPrs773569201
dbSNP (classic)rs773569201
ClinGenrs773569201
ebirs773569201
HLIrs773569201
Exacrs773569201
Gnomadrs773569201
Varsomers773569201
LitVarrs773569201
Maprs773569201
PheGenIrs773569201
Biobankrs773569201
1000 genomesrs773569201
hgdprs773569201
ensemblrs773569201
geneviewrs773569201
scholarrs773569201
googlers773569201
pharmgkbrs773569201
gwascentralrs773569201
openSNPrs773569201
23andMers773569201
23andMe allrs773569201
SNPshotrs773569201
SNPdbers773569201
MSV3drs773569201
GWAS Ctlgrs773569201
Max Magnitude0

aka c.1724T>A, p.Phe575Tyr or F575Y

In the CFTR2 database, the minor allele is considered to be of varying clinical consequence. In a functional study, it shows 17.1% of wild-type CFTR activity.[PMID 29805046OA-icon.png]