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rs397508433

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397508433(-;-)
Make rs397508433(-;TT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117603649
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508433
dbSNP (old)rs397508433
ClinGenrs397508433
ebirs397508433
HLIrs397508433
Exacrs397508433
Gnomadrs397508433
Varsomers397508433
Maprs397508433
PheGenIrs397508433
Biobankrs397508433
1000 genomesrs397508433
hgdprs397508433
ensemblrs397508433
gopubmedrs397508433
geneviewrs397508433
scholarrs397508433
googlers397508433
pharmgkbrs397508433
gwascentralrs397508433
openSNPrs397508433
23andMers397508433
23andMe allrs397508433
SNP Nexus

SNPshotrs397508433
SNPdbers397508433
MSV3drs397508433
GWAS Ctlgrs397508433
Max Magnitude0
ClinVar
Risk rs397508433(-;-)
Alt rs397508433(-;-)
Reference Rs397508433(TT;TT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117243703_117243704delTT
CLNSRC ClinVar
CLNACC RCV000046687.2,