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rs397508664

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs397508664(-;-)
Make rs397508664(-;GC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117664764
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508664
ebirs397508664
HLIrs397508664
Exacrs397508664
Varsomers397508664
Maprs397508664
PheGenIrs397508664
hapmaprs397508664
1000 genomesrs397508664
hgdprs397508664
ensemblrs397508664
gopubmedrs397508664
geneviewrs397508664
scholarrs397508664
googlers397508664
pharmgkbrs397508664
gwascentralrs397508664
openSNPrs397508664
23andMers397508664
23andMe allrs397508664
SNP Nexus

SNPshotrs397508664
SNPdbers397508664
MSV3drs397508664
GWAS Ctlgrs397508664
Max Magnitude0
ClinVar
Risk rs397508664(;)
Alt rs397508664(;)
Reference rs397508664(GC;GC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117304818_117304819delGC
CLNSRC ClinVar
CLNACC RCV000047061.2,