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rs397508727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508727(A;A)
Make rs397508727(A;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531101
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508727
ebirs397508727
HLIrs397508727
Exacrs397508727
Varsomers397508727
Maprs397508727
PheGenIrs397508727
hapmaprs397508727
1000 genomesrs397508727
hgdprs397508727
ensemblrs397508727
gopubmedrs397508727
geneviewrs397508727
scholarrs397508727
googlers397508727
pharmgkbrs397508727
gwascentralrs397508727
openSNPrs397508727
23andMers397508727
23andMe allrs397508727
SNP Nexus

SNPshotrs397508727
SNPdbers397508727
MSV3drs397508727
GWAS Ctlgrs397508727
Max Magnitude0
ClinVar
Risk rs397508727(A,C;A,C)
Alt rs397508727(A,C;A,C)
Reference rs397508727(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171155T>A; NC_000007.13:g.117171155T>C
CLNSRC ClinVar
CLNACC RCV000047151.2, RCV000047152.2,