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rs397508356

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCTCGCAT;CCTCGCAT) 0 common in clinvar
Make rs397508356(-;-)
Make rs397508356(-;CCTCGCAT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592415
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508356
ebirs397508356
HLIrs397508356
Exacrs397508356
Varsomers397508356
Maprs397508356
PheGenIrs397508356
hapmaprs397508356
1000 genomesrs397508356
hgdprs397508356
ensemblrs397508356
gopubmedrs397508356
geneviewrs397508356
scholarrs397508356
googlers397508356
pharmgkbrs397508356
gwascentralrs397508356
openSNPrs397508356
23andMers397508356
23andMe allrs397508356
SNP Nexus

SNPshotrs397508356
SNPdbers397508356
MSV3drs397508356
GWAS Ctlgrs397508356
Max Magnitude0
ClinVar
Risk rs397508356(;)
Alt rs397508356(;)
Reference rs397508356(CCTCGCAT;CCTCGCAT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232469_117232476delCCTCGCAT
CLNSRC ClinVar
CLNACC RCV000046560.2,