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rs397508344

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AA;AA) 0 common in clinvar
Make rs397508344(AA;GT)
Make rs397508344(GT;GT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592312
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508344
ebirs397508344
HLIrs397508344
Exacrs397508344
Varsomers397508344
Maprs397508344
PheGenIrs397508344
hapmaprs397508344
1000 genomesrs397508344
hgdprs397508344
ensemblrs397508344
gopubmedrs397508344
geneviewrs397508344
scholarrs397508344
googlers397508344
pharmgkbrs397508344
gwascentralrs397508344
openSNPrs397508344
23andMers397508344
23andMe allrs397508344
SNP Nexus

SNPshotrs397508344
SNPdbers397508344
MSV3drs397508344
GWAS Ctlgrs397508344
Max Magnitude0
ClinVar
Risk rs397508344(GT;GT)
Alt rs397508344(GT;GT)
Reference rs397508344(AA;AA)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232366_117232367delAAinsGT
CLNSRC ClinVar
CLNACC RCV000046542.2,