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rs397508566

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508566(-;-)
Make rs397508566(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117614690
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508566
ebirs397508566
HLIrs397508566
Exacrs397508566
Varsomers397508566
Maprs397508566
PheGenIrs397508566
hapmaprs397508566
1000 genomesrs397508566
hgdprs397508566
ensemblrs397508566
gopubmedrs397508566
geneviewrs397508566
scholarrs397508566
googlers397508566
pharmgkbrs397508566
gwascentralrs397508566
openSNPrs397508566
23andMers397508566
23andMe allrs397508566
SNP Nexus

SNPshotrs397508566
SNPdbers397508566
MSV3drs397508566
GWAS Ctlgrs397508566
Max Magnitude0
ClinVar
Risk rs397508566(;)
Alt rs397508566(;)
Reference rs397508566(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117254744delT
CLNSRC ClinVar
CLNACC RCV000046894.2,