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rs397508496

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508496(C;T)
Make rs397508496(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610633
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508496
ebirs397508496
HLIrs397508496
Exacrs397508496
Varsomers397508496
Maprs397508496
PheGenIrs397508496
hapmaprs397508496
1000 genomesrs397508496
hgdprs397508496
ensemblrs397508496
gopubmedrs397508496
geneviewrs397508496
scholarrs397508496
googlers397508496
pharmgkbrs397508496
gwascentralrs397508496
openSNPrs397508496
23andMers397508496
23andMe allrs397508496
SNP Nexus

SNPshotrs397508496
SNPdbers397508496
MSV3drs397508496
GWAS Ctlgrs397508496
Max Magnitude0
ClinVar
Risk rs397508496(T;T)
Alt rs397508496(T;T)
Reference rs397508496(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250687C>T
CLNSRC ClinVar
CLNACC RCV000046781.2,