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rs397508690

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508690(-;-)
Make rs397508690(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117665492
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508690
ebirs397508690
HLIrs397508690
Exacrs397508690
Varsomers397508690
Maprs397508690
PheGenIrs397508690
hapmaprs397508690
1000 genomesrs397508690
hgdprs397508690
ensemblrs397508690
gopubmedrs397508690
geneviewrs397508690
scholarrs397508690
googlers397508690
pharmgkbrs397508690
gwascentralrs397508690
openSNPrs397508690
23andMers397508690
23andMe allrs397508690
SNP Nexus

SNPshotrs397508690
SNPdbers397508690
MSV3drs397508690
GWAS Ctlgrs397508690
Max Magnitude0
ClinVar
Risk rs397508690(;)
Alt rs397508690(;)
Reference rs397508690(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117305546delA
CLNSRC ClinVar
CLNACC RCV000047096.2,