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rs397508336

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 3 carrier of a cystic fibrosis allele
Make rs397508336(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592220
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508336
ebirs397508336
HLIrs397508336
Exacrs397508336
Varsomers397508336
Maprs397508336
PheGenIrs397508336
hapmaprs397508336
1000 genomesrs397508336
hgdprs397508336
ensemblrs397508336
gopubmedrs397508336
geneviewrs397508336
scholarrs397508336
googlers397508336
pharmgkbrs397508336
gwascentralrs397508336
openSNPrs397508336
23andMers397508336
23andMe allrs397508336
SNP Nexus

SNPshotrs397508336
SNPdbers397508336
MSV3drs397508336
GWAS Ctlgrs397508336
Max Magnitude3
ClinVar
Risk rs397508336(T;T)
Alt rs397508336(T;T)
Reference rs397508336(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232274C>T
CLNSRC CFTR2
CLNACC RCV000046532.3,