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rs397508760

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAGTATG;AAGTATG) 0 common in clinvar
(ATGAAGT;ATGAAGT) 0 common in clinvar
Make rs397508760(-;-)
Make rs397508760(-;AAGTATG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534364
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508760
ebirs397508760
HLIrs397508760
Exacrs397508760
Varsomers397508760
Maprs397508760
PheGenIrs397508760
hapmaprs397508760
1000 genomesrs397508760
hgdprs397508760
ensemblrs397508760
gopubmedrs397508760
geneviewrs397508760
scholarrs397508760
googlers397508760
pharmgkbrs397508760
gwascentralrs397508760
openSNPrs397508760
23andMers397508760
23andMe allrs397508760
SNP Nexus

SNPshotrs397508760
SNPdbers397508760
MSV3drs397508760
GWAS Ctlgrs397508760
Max Magnitude0
ClinVar
Risk rs397508760(;)
Alt rs397508760(;)
Reference rs397508760(ATGAAGT;ATGAAGT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174418_117174424delAAGTATG
CLNSRC ClinVar
CLNACC RCV000047200.2,