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rs397508143

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397508143(-;-)
Make rs397508143(-;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117540248
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508143
ebirs397508143
HLIrs397508143
Exacrs397508143
Varsomers397508143
Maprs397508143
PheGenIrs397508143
hapmaprs397508143
1000 genomesrs397508143
hgdprs397508143
ensemblrs397508143
gopubmedrs397508143
geneviewrs397508143
scholarrs397508143
googlers397508143
pharmgkbrs397508143
gwascentralrs397508143
openSNPrs397508143
23andMers397508143
23andMe allrs397508143
SNP Nexus

SNPshotrs397508143
SNPdbers397508143
MSV3drs397508143
GWAS Ctlgrs397508143
Max Magnitude0
ClinVar
Risk rs397508143(;)
Alt rs397508143(;)
Reference rs397508143(A;A)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117180302delA
CLNSRC ClinVar
CLNACC RCV000046200.2,