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rs397508806

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTTAA;CTTAA) 0 common in clinvar
Make rs397508806(-;-)
Make rs397508806(-;CTTAA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117536665
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508806
ebirs397508806
HLIrs397508806
Exacrs397508806
Varsomers397508806
Maprs397508806
PheGenIrs397508806
hapmaprs397508806
1000 genomesrs397508806
hgdprs397508806
ensemblrs397508806
gopubmedrs397508806
geneviewrs397508806
scholarrs397508806
googlers397508806
pharmgkbrs397508806
gwascentralrs397508806
openSNPrs397508806
23andMers397508806
23andMe allrs397508806
SNP Nexus

SNPshotrs397508806
SNPdbers397508806
MSV3drs397508806
GWAS Ctlgrs397508806
Max Magnitude0
ClinVar
Risk rs397508806(;)
Alt rs397508806(;)
Reference rs397508806(AACTT;AACTT)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176719_117176723delCTTAA
CLNSRC CFTR2
CLNACC RCV000047272.5,