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rs397508149

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397508149(-;-)
Make rs397508149(-;A)
Make rs397508149(A;A)
ReferenceGRCh38 38.1/141
Chromosome7
Position117504304
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508149
ebirs397508149
HLIrs397508149
Exacrs397508149
Varsomers397508149
Maprs397508149
PheGenIrs397508149
hapmaprs397508149
1000 genomesrs397508149
hgdprs397508149
ensemblrs397508149
gopubmedrs397508149
geneviewrs397508149
scholarrs397508149
googlers397508149
pharmgkbrs397508149
gwascentralrs397508149
openSNPrs397508149
23andMers397508149
23andMe allrs397508149
SNP Nexus

SNPshotrs397508149
SNPdbers397508149
MSV3drs397508149
GWAS Ctlgrs397508149
Max Magnitude0
ClinVar
Risk rs397508149(A;A)
Alt rs397508149(A;A)
Reference rs397508149(;)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117144358dupA
CLNSRC ClinVar
CLNACC RCV000046217.2,