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rs397508647

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508647(-;-)
Make rs397508647(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531018
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508647
ebirs397508647
HLIrs397508647
Exacrs397508647
Varsomers397508647
Maprs397508647
PheGenIrs397508647
hapmaprs397508647
1000 genomesrs397508647
hgdprs397508647
ensemblrs397508647
gopubmedrs397508647
geneviewrs397508647
scholarrs397508647
googlers397508647
pharmgkbrs397508647
gwascentralrs397508647
openSNPrs397508647
23andMers397508647
23andMe allrs397508647
SNP Nexus

SNPshotrs397508647
SNPdbers397508647
MSV3drs397508647
GWAS Ctlgrs397508647
Max Magnitude0
ClinVar
Risk rs397508647(;)
Alt rs397508647(;)
Reference rs397508647(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171072delT
CLNSRC ClinVar
CLNACC RCV000047040.2,