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rs397508367

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508367(-;-)
Make rs397508367(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117509102
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508367
ClinGenrs397508367
ebirs397508367
HLIrs397508367
Exacrs397508367
Varsomers397508367
Maprs397508367
PheGenIrs397508367
hapmaprs397508367
1000 genomesrs397508367
hgdprs397508367
ensemblrs397508367
gopubmedrs397508367
geneviewrs397508367
scholarrs397508367
googlers397508367
pharmgkbrs397508367
gwascentralrs397508367
openSNPrs397508367
23andMers397508367
23andMe allrs397508367
SNP Nexus

SNPshotrs397508367
SNPdbers397508367
MSV3drs397508367
GWAS Ctlgrs397508367
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397508367(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117149156delT
CLNSRC ClinVar
CLNACC RCV000046578.2,