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rs397508743

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ATAAA;ATAAA) 0 common in clinvar
Make rs397508743(-;-)
Make rs397508743(-;ATAAA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117534304
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508743
ebirs397508743
HLIrs397508743
Exacrs397508743
Varsomers397508743
Maprs397508743
PheGenIrs397508743
hapmaprs397508743
1000 genomesrs397508743
hgdprs397508743
ensemblrs397508743
gopubmedrs397508743
geneviewrs397508743
scholarrs397508743
googlers397508743
pharmgkbrs397508743
gwascentralrs397508743
openSNPrs397508743
23andMers397508743
23andMe allrs397508743
SNP Nexus

SNPshotrs397508743
SNPdbers397508743
MSV3drs397508743
GWAS Ctlgrs397508743
Max Magnitude0
ClinVar
Risk rs397508743(;)
Alt rs397508743(;)
Reference rs397508743(ATAAA;ATAAA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117174358_117174362delATAAA
CLNSRC ClinVar
CLNACC RCV000047176.2,