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rs397508443

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508443(A;T)
Make rs397508443(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603710
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508443
ebirs397508443
HLIrs397508443
Exacrs397508443
Varsomers397508443
Maprs397508443
PheGenIrs397508443
hapmaprs397508443
1000 genomesrs397508443
hgdprs397508443
ensemblrs397508443
gopubmedrs397508443
geneviewrs397508443
scholarrs397508443
googlers397508443
pharmgkbrs397508443
gwascentralrs397508443
openSNPrs397508443
23andMers397508443
23andMe allrs397508443
SNP Nexus

SNPshotrs397508443
SNPdbers397508443
MSV3drs397508443
GWAS Ctlgrs397508443
Max Magnitude0
ClinVar
Risk rs397508443(T;T)
Alt rs397508443(T;T)
Reference rs397508443(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243764A>T
CLNSRC ClinVar
CLNACC RCV000046698.2,