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rs397508239

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs397508239(-;-)
Make rs397508239(-;AC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117587764
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508239
ebirs397508239
HLIrs397508239
Exacrs397508239
Varsomers397508239
Maprs397508239
PheGenIrs397508239
hapmaprs397508239
1000 genomesrs397508239
hgdprs397508239
ensemblrs397508239
gopubmedrs397508239
geneviewrs397508239
scholarrs397508239
googlers397508239
pharmgkbrs397508239
gwascentralrs397508239
openSNPrs397508239
23andMers397508239
23andMe allrs397508239
SNP Nexus

SNPshotrs397508239
SNPdbers397508239
MSV3drs397508239
GWAS Ctlgrs397508239
Max Magnitude0
ClinVar
Risk rs397508239(;)
Alt rs397508239(;)
Reference rs397508239(AC;AC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117227818_117227819delAC
CLNSRC ClinVar
CLNACC RCV000046361.2,