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rs397508605

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508605(-;-)
Make rs397508605(-;C)
Make rs397508605(C;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642486
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508605
ebirs397508605
HLIrs397508605
Exacrs397508605
Varsomers397508605
Maprs397508605
PheGenIrs397508605
hapmaprs397508605
1000 genomesrs397508605
hgdprs397508605
ensemblrs397508605
gopubmedrs397508605
geneviewrs397508605
scholarrs397508605
googlers397508605
pharmgkbrs397508605
gwascentralrs397508605
openSNPrs397508605
23andMers397508605
23andMe allrs397508605
SNP Nexus

SNPshotrs397508605
SNPdbers397508605
MSV3drs397508605
GWAS Ctlgrs397508605
Max Magnitude0
ClinVar
Risk rs397508605(C;C)
Alt rs397508605(C;C)
Reference rs397508605(;)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282541dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000007598.3,