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rs397508209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508209(-;-)
Make rs397508209(-;T)
Make rs397508209(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559515
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508209
ebirs397508209
HLIrs397508209
Exacrs397508209
Varsomers397508209
Maprs397508209
PheGenIrs397508209
hapmaprs397508209
1000 genomesrs397508209
hgdprs397508209
ensemblrs397508209
gopubmedrs397508209
geneviewrs397508209
scholarrs397508209
googlers397508209
pharmgkbrs397508209
gwascentralrs397508209
openSNPrs397508209
23andMers397508209
23andMe allrs397508209
SNP Nexus

SNPshotrs397508209
SNPdbers397508209
MSV3drs397508209
GWAS Ctlgrs397508209
Max Magnitude0
ClinVar
Risk rs397508209(T;T)
Alt rs397508209(T;T)
Reference rs397508209(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199570dupT
CLNSRC ClinVar
CLNACC RCV000046306.2,