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rs397508331

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 carrier of a cystic fibrosis allele
Make rs397508331(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592184
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508331
ebirs397508331
HLIrs397508331
Exacrs397508331
Varsomers397508331
Maprs397508331
PheGenIrs397508331
hapmaprs397508331
1000 genomesrs397508331
hgdprs397508331
ensemblrs397508331
gopubmedrs397508331
geneviewrs397508331
scholarrs397508331
googlers397508331
pharmgkbrs397508331
gwascentralrs397508331
openSNPrs397508331
23andMers397508331
23andMe allrs397508331
SNP Nexus

SNPshotrs397508331
SNPdbers397508331
MSV3drs397508331
GWAS Ctlgrs397508331
Max Magnitude3
ClinVar
Risk rs397508331(T;T)
Alt rs397508331(T;T)
Reference rs397508331(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232238G>T
CLNSRC CFTR2
CLNACC RCV000046523.3,