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rs397508396

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397508396(-;-)
Make rs397508396(-;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position117595001
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508396
ebirs397508396
HLIrs397508396
Exacrs397508396
Varsomers397508396
Maprs397508396
PheGenIrs397508396
hapmaprs397508396
1000 genomesrs397508396
hgdprs397508396
ensemblrs397508396
gopubmedrs397508396
geneviewrs397508396
scholarrs397508396
googlers397508396
pharmgkbrs397508396
gwascentralrs397508396
openSNPrs397508396
23andMers397508396
23andMe allrs397508396
SNP Nexus

SNPshotrs397508396
SNPdbers397508396
MSV3drs397508396
GWAS Ctlgrs397508396
Max Magnitude0
ClinVar
Risk rs397508396(;)
Alt rs397508396(;)
Reference rs397508396(T;T)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117235055delT
CLNSRC ClinVar
CLNACC RCV000046620.2,