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rs397508684

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508684(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117665466
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508684
ebirs397508684
HLIrs397508684
Exacrs397508684
Varsomers397508684
Maprs397508684
PheGenIrs397508684
hapmaprs397508684
1000 genomesrs397508684
hgdprs397508684
ensemblrs397508684
gopubmedrs397508684
geneviewrs397508684
scholarrs397508684
googlers397508684
pharmgkbrs397508684
gwascentralrs397508684
openSNPrs397508684
23andMers397508684
23andMe allrs397508684
SNP Nexus

SNPshotrs397508684
SNPdbers397508684
MSV3drs397508684
GWAS Ctlgrs397508684
Max Magnitude0
ClinVar
Risk rs397508684(A,T;A,T)
Alt rs397508684(A,T;A,T)
Reference rs397508684(C;C)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117305520C>T
CLNSRC CFTR2
CLNACC RCV000047087.3,