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rs397508671

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTCC;CTCC) 0 common in clinvar
Make rs397508671(-;-)
Make rs397508671(-;CTCC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531034
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508671
ebirs397508671
HLIrs397508671
Exacrs397508671
Varsomers397508671
Maprs397508671
PheGenIrs397508671
hapmaprs397508671
1000 genomesrs397508671
hgdprs397508671
ensemblrs397508671
gopubmedrs397508671
geneviewrs397508671
scholarrs397508671
googlers397508671
pharmgkbrs397508671
gwascentralrs397508671
openSNPrs397508671
23andMers397508671
23andMe allrs397508671
SNP Nexus

SNPshotrs397508671
SNPdbers397508671
MSV3drs397508671
GWAS Ctlgrs397508671
Max Magnitude0
ClinVar
Risk rs397508671(;)
Alt rs397508671(;)
Reference rs397508671(CTCC;CTCC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171088_117171091delCTCC
CLNSRC ClinVar
CLNACC RCV000047071.2,