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rs397508549

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508549(A;T)
Make rs397508549(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614627
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508549
ebirs397508549
HLIrs397508549
Exacrs397508549
Varsomers397508549
Maprs397508549
PheGenIrs397508549
hapmaprs397508549
1000 genomesrs397508549
hgdprs397508549
ensemblrs397508549
gopubmedrs397508549
geneviewrs397508549
scholarrs397508549
googlers397508549
pharmgkbrs397508549
gwascentralrs397508549
openSNPrs397508549
23andMers397508549
23andMe allrs397508549
SNP Nexus

SNPshotrs397508549
SNPdbers397508549
MSV3drs397508549
GWAS Ctlgrs397508549
Max Magnitude0
ClinVar
Risk rs397508549(T;T)
Alt rs397508549(T;T)
Reference rs397508549(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254681A>T
CLNSRC ClinVar
CLNACC RCV000046877.2,