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rs397508695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs397508695(-;-)
Make rs397508695(-;TG)
ReferenceGRCh38 38.1/141
Chromosome7
Position117665522
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508695
ebirs397508695
HLIrs397508695
Exacrs397508695
Varsomers397508695
Maprs397508695
PheGenIrs397508695
hapmaprs397508695
1000 genomesrs397508695
hgdprs397508695
ensemblrs397508695
gopubmedrs397508695
geneviewrs397508695
scholarrs397508695
googlers397508695
pharmgkbrs397508695
gwascentralrs397508695
openSNPrs397508695
23andMers397508695
23andMe allrs397508695
SNP Nexus

SNPshotrs397508695
SNPdbers397508695
MSV3drs397508695
GWAS Ctlgrs397508695
Max Magnitude0
ClinVar
Risk rs397508695(;)
Alt rs397508695(;)
Reference rs397508695(TG;TG)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117305576_117305577delTG
CLNSRC ClinVar
CLNACC RCV000047102.2,