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rs397508807

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTAAGACAG;TTAAGACAG) 0 common in clinvar
Make rs397508807(-;-)
Make rs397508807(-;TTAAGACAG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117536666
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508807
ebirs397508807
HLIrs397508807
Exacrs397508807
Varsomers397508807
Maprs397508807
PheGenIrs397508807
hapmaprs397508807
1000 genomesrs397508807
hgdprs397508807
ensemblrs397508807
gopubmedrs397508807
geneviewrs397508807
scholarrs397508807
googlers397508807
pharmgkbrs397508807
gwascentralrs397508807
openSNPrs397508807
23andMers397508807
23andMe allrs397508807
SNP Nexus

SNPshotrs397508807
SNPdbers397508807
MSV3drs397508807
GWAS Ctlgrs397508807
Max Magnitude0
ClinVar
Risk rs397508807(;)
Alt rs397508807(;)
Reference rs397508807(TTAAGACAG;TTAAGACAG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176720_117176728delTTAAGACAG
CLNSRC ClinVar
CLNACC RCV000047273.2,