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rs397508493

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TAGTG;TAGTG) 0 common in clinvar
Make rs397508493(-;-)
Make rs397508493(-;TAGTG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117610598
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508493
ebirs397508493
HLIrs397508493
Exacrs397508493
Varsomers397508493
Maprs397508493
PheGenIrs397508493
hapmaprs397508493
1000 genomesrs397508493
hgdprs397508493
ensemblrs397508493
gopubmedrs397508493
geneviewrs397508493
scholarrs397508493
googlers397508493
pharmgkbrs397508493
gwascentralrs397508493
openSNPrs397508493
23andMers397508493
23andMe allrs397508493
SNP Nexus

SNPshotrs397508493
SNPdbers397508493
MSV3drs397508493
GWAS Ctlgrs397508493
Max Magnitude0
ClinVar
Risk rs397508493(;)
Alt rs397508493(;)
Reference rs397508493(TAGTG;TAGTG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117250652_117250656delTAGTG
CLNSRC ClinVar
CLNACC RCV000046776.2,