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rs397508169

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACGACTA;ACGACTA) 0 common in clinvar
(TAACGAC;TAACGAC) 0 common in clinvar
Make rs397508169(-;-)
Make rs397508169(-;ACGACTA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117542061
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508169
ClinGenrs397508169
ebirs397508169
HLIrs397508169
Exacrs397508169
Varsomers397508169
Maprs397508169
PheGenIrs397508169
hapmaprs397508169
1000 genomesrs397508169
hgdprs397508169
ensemblrs397508169
gopubmedrs397508169
geneviewrs397508169
scholarrs397508169
googlers397508169
pharmgkbrs397508169
gwascentralrs397508169
openSNPrs397508169
23andMers397508169
23andMe allrs397508169
SNP Nexus

SNPshotrs397508169
SNPdbers397508169
MSV3drs397508169
GWAS Ctlgrs397508169
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs397508169(TAACGAC;TAACGAC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117182115_117182121delACGACTA
CLNSRC ClinVar
CLNACC RCV000046249.2,