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rs397508186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TTCTCAC;TTCTCAC) 0 common in clinvar
Make rs397508186(-;-)
Make rs397508186(-;TTCTCAC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117548728
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508186
ebirs397508186
HLIrs397508186
Exacrs397508186
Varsomers397508186
Maprs397508186
PheGenIrs397508186
hapmaprs397508186
1000 genomesrs397508186
hgdprs397508186
ensemblrs397508186
gopubmedrs397508186
geneviewrs397508186
scholarrs397508186
googlers397508186
pharmgkbrs397508186
gwascentralrs397508186
openSNPrs397508186
23andMers397508186
23andMe allrs397508186
SNP Nexus

SNPshotrs397508186
SNPdbers397508186
MSV3drs397508186
GWAS Ctlgrs397508186
Max Magnitude0
ClinVar
Risk rs397508186(;)
Alt rs397508186(;)
Reference rs397508186(TTCTCAC;TTCTCAC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188782_117188788delTTCTCAC
CLNSRC ClinVar
CLNACC RCV000046270.2,