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rs397508698

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508698(-;-)
Make rs397508698(-;A)
Make rs397508698(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531045
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508698
ebirs397508698
HLIrs397508698
Exacrs397508698
Varsomers397508698
Maprs397508698
PheGenIrs397508698
hapmaprs397508698
1000 genomesrs397508698
hgdprs397508698
ensemblrs397508698
gopubmedrs397508698
geneviewrs397508698
scholarrs397508698
googlers397508698
pharmgkbrs397508698
gwascentralrs397508698
openSNPrs397508698
23andMers397508698
23andMe allrs397508698
SNP Nexus

SNPshotrs397508698
SNPdbers397508698
MSV3drs397508698
GWAS Ctlgrs397508698
Max Magnitude0
ClinVar
Risk rs397508698(A;A)
Alt rs397508698(A;A)
Reference rs397508698(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171099dupA
CLNSRC ClinVar
CLNACC RCV000047107.2,