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rs397508662

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCTAAGC;CCTAAGC) 0 common in clinvar
(CTAAGCC;CTAAGCC) 0 common in clinvar
Make rs397508662(-;-)
Make rs397508662(-;CTAAGCC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664760
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508662
ebirs397508662
HLIrs397508662
Exacrs397508662
Varsomers397508662
Maprs397508662
PheGenIrs397508662
hapmaprs397508662
1000 genomesrs397508662
hgdprs397508662
ensemblrs397508662
gopubmedrs397508662
geneviewrs397508662
scholarrs397508662
googlers397508662
pharmgkbrs397508662
gwascentralrs397508662
openSNPrs397508662
23andMers397508662
23andMe allrs397508662
SNP Nexus

SNPshotrs397508662
SNPdbers397508662
MSV3drs397508662
GWAS Ctlgrs397508662
Max Magnitude0
ClinVar
Risk rs397508662(;)
Alt rs397508662(;)
Reference rs397508662(CCTAAGC;CCTAAGC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304814_117304820delCTAAGCC
CLNSRC ClinVar
CLNACC RCV000047059.2,