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rs397508341

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508341(-;-)
Make rs397508341(-;A)
Make rs397508341(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117592256
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508341
ebirs397508341
HLIrs397508341
Exacrs397508341
Varsomers397508341
Maprs397508341
PheGenIrs397508341
hapmaprs397508341
1000 genomesrs397508341
hgdprs397508341
ensemblrs397508341
gopubmedrs397508341
geneviewrs397508341
scholarrs397508341
googlers397508341
pharmgkbrs397508341
gwascentralrs397508341
openSNPrs397508341
23andMers397508341
23andMe allrs397508341
SNP Nexus

SNPshotrs397508341
SNPdbers397508341
MSV3drs397508341
GWAS Ctlgrs397508341
Max Magnitude0
ClinVar
Risk rs397508341(A;A)
Alt rs397508341(A;A)
Reference rs397508341(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232310dupA
CLNSRC ClinVar
CLNACC RCV000046537.2,