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rs397508805

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;AACTT) 3 carrier of a cystic fibrosis allele
(AACTT;AACTT) 0 common in clinvar


Make rs397508805(-;-)
ReferenceGRCh38 38.1/141
Chromosome7
Position117536663
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508805
dbSNP (classic)rs397508805
ClinGenrs397508805
ebirs397508805
HLIrs397508805
Exacrs397508805
Gnomadrs397508805
Varsomers397508805
LitVarrs397508805
Maprs397508805
PheGenIrs397508805
Biobankrs397508805
1000 genomesrs397508805
hgdprs397508805
ensemblrs397508805
geneviewrs397508805
scholarrs397508805
googlers397508805
pharmgkbrs397508805
gwascentralrs397508805
openSNPrs397508805
23andMers397508805
SNPshotrs397508805
SNPdbers397508805
MSV3drs397508805
GWAS Ctlgrs397508805
Merged fromRs397508806
Max Magnitude3
ClinVar
Risk rs397508805(-;-) rs397508805(CTTAA;CTTAA)
Alt rs397508805(-;-) rs397508805(CTTAA;CTTAA)
Reference Rs397508805(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,