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rs397508687

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508687(-;-)
Make rs397508687(-;GA)
Make rs397508687(GA;GA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117531040
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508687
ebirs397508687
HLIrs397508687
Exacrs397508687
Varsomers397508687
Maprs397508687
PheGenIrs397508687
hapmaprs397508687
1000 genomesrs397508687
hgdprs397508687
ensemblrs397508687
gopubmedrs397508687
geneviewrs397508687
scholarrs397508687
googlers397508687
pharmgkbrs397508687
gwascentralrs397508687
openSNPrs397508687
23andMers397508687
23andMe allrs397508687
SNP Nexus

SNPshotrs397508687
SNPdbers397508687
MSV3drs397508687
GWAS Ctlgrs397508687
Max Magnitude0
ClinVar
Risk rs397508687(GA;GA)
Alt rs397508687(GA;GA)
Reference rs397508687(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117171094_117171095insGA
CLNSRC ClinVar
CLNACC RCV000047091.2,