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rs397508614

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508614(-;-)
Make rs397508614(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642549
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508614
ebirs397508614
HLIrs397508614
Exacrs397508614
Varsomers397508614
Maprs397508614
PheGenIrs397508614
hapmaprs397508614
1000 genomesrs397508614
hgdprs397508614
ensemblrs397508614
gopubmedrs397508614
geneviewrs397508614
scholarrs397508614
googlers397508614
pharmgkbrs397508614
gwascentralrs397508614
openSNPrs397508614
23andMers397508614
23andMe allrs397508614
SNP Nexus

SNPshotrs397508614
SNPdbers397508614
MSV3drs397508614
GWAS Ctlgrs397508614
Max Magnitude0
ClinVar
Risk rs397508614(;)
Alt rs397508614(;)
Reference rs397508614(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282603delA
CLNSRC ClinVar
CLNACC RCV000046990.2,