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rs397508543

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508543(-;-)
Make rs397508543(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117611805
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508543
ebirs397508543
HLIrs397508543
Exacrs397508543
Varsomers397508543
Maprs397508543
PheGenIrs397508543
hapmaprs397508543
1000 genomesrs397508543
hgdprs397508543
ensemblrs397508543
gopubmedrs397508543
geneviewrs397508543
scholarrs397508543
googlers397508543
pharmgkbrs397508543
gwascentralrs397508543
openSNPrs397508543
23andMers397508543
23andMe allrs397508543
SNP Nexus

SNPshotrs397508543
SNPdbers397508543
MSV3drs397508543
GWAS Ctlgrs397508543
Max Magnitude0
ClinVar
Risk rs397508543(;)
Alt rs397508543(;)
Reference rs397508543(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117251859delA
CLNSRC ClinVar
CLNACC RCV000046871.2,