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rs397508215

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397508215(-;-)
Make rs397508215(-;TT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117559553
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508215
ebirs397508215
HLIrs397508215
Exacrs397508215
Varsomers397508215
Maprs397508215
PheGenIrs397508215
hapmaprs397508215
1000 genomesrs397508215
hgdprs397508215
ensemblrs397508215
gopubmedrs397508215
geneviewrs397508215
scholarrs397508215
googlers397508215
pharmgkbrs397508215
gwascentralrs397508215
openSNPrs397508215
23andMers397508215
23andMe allrs397508215
SNP Nexus

SNPshotrs397508215
SNPdbers397508215
MSV3drs397508215
GWAS Ctlgrs397508215
Max Magnitude0
ClinVar
Risk rs397508215(;)
Alt rs397508215(;)
Reference rs397508215(TT;TT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117199607_117199608delTT
CLNSRC ClinVar
CLNACC RCV000046317.2,