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rs146795445

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs146795445(C;C)
Make rs146795445(C;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642595
GeneCFTR
is asnp
is mentioned by
dbSNPrs146795445
ebirs146795445
HLIrs146795445
Exacrs146795445
Varsomers146795445
Maprs146795445
PheGenIrs146795445
hapmaprs146795445
1000 genomesrs146795445
hgdprs146795445
ensemblrs146795445
gopubmedrs146795445
geneviewrs146795445
scholarrs146795445
googlers146795445
pharmgkbrs146795445
gwascentralrs146795445
openSNPrs146795445
23andMers146795445
23andMe allrs146795445
SNP Nexus

SNPshotrs146795445
SNPdbers146795445
MSV3drs146795445
GWAS Ctlgrs146795445
Max Magnitude0
ClinVar
Risk rs146795445(C;C)
Alt rs146795445(C;C)
Reference rs146795445(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282649T>C
CLNSRC ClinVar
CLNACC RCV000047004.2,