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rs397508401

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TT;TT) 0 common in clinvar
Make rs397508401(-;-)
Make rs397508401(-;TT)
ReferenceGRCh38 38.1/141
Chromosome7
Position117595030
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508401
ebirs397508401
HLIrs397508401
Exacrs397508401
Varsomers397508401
Maprs397508401
PheGenIrs397508401
hapmaprs397508401
1000 genomesrs397508401
hgdprs397508401
ensemblrs397508401
gopubmedrs397508401
geneviewrs397508401
scholarrs397508401
googlers397508401
pharmgkbrs397508401
gwascentralrs397508401
openSNPrs397508401
23andMers397508401
23andMe allrs397508401
SNP Nexus

SNPshotrs397508401
SNPdbers397508401
MSV3drs397508401
GWAS Ctlgrs397508401
Max Magnitude0
ClinVar
Risk rs397508401(;)
Alt rs397508401(;)
Reference rs397508401(TT;TT)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117235084_117235085delTT
CLNSRC ClinVar
CLNACC RCV000046625.2,