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rs186045772

From SNPedia

Cystic Fibrosis related
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;T) 3 Carrier for a cystic fibrosis allele
(T;T) 0 common/normal


Make rs186045772(A;A)
ReferenceGRCh38 38.1/142
Chromosome7
Position117611663
GeneCFTR
is asnp
is mentioned by
dbSNPrs186045772
ebirs186045772
HLIrs186045772
Exacrs186045772
Varsomers186045772
Maprs186045772
PheGenIrs186045772
hapmaprs186045772
1000 genomesrs186045772
hgdprs186045772
ensemblrs186045772
gopubmedrs186045772
geneviewrs186045772
scholarrs186045772
googlers186045772
pharmgkbrs186045772
gwascentralrs186045772
openSNPrs186045772
23andMers186045772
23andMe allrs186045772
SNP Nexus

SNPshotrs186045772
SNPdbers186045772
MSV3drs186045772
GWAS Ctlgrs186045772
Max Magnitude3
Cystic fibrosis; c.3222T>A, p.Phe1074Leu

named i5011834 by 23andMe

ClinVar
Risk rs186045772(A;A)
Alt rs186045772(A;A)
Reference rs186045772(T;T)
Significance Probable-Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251717T>A
CLNSRC
CLNACC RCV000046829.3,