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rs397508301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs397508301(-;-)
Make rs397508301(-;GC)
ReferenceGRCh38 38.1/141
Chromosome7
Position117591953
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508301
ebirs397508301
HLIrs397508301
Exacrs397508301
Varsomers397508301
Maprs397508301
PheGenIrs397508301
hapmaprs397508301
1000 genomesrs397508301
hgdprs397508301
ensemblrs397508301
gopubmedrs397508301
geneviewrs397508301
scholarrs397508301
googlers397508301
pharmgkbrs397508301
gwascentralrs397508301
openSNPrs397508301
23andMers397508301
23andMe allrs397508301
SNP Nexus

SNPshotrs397508301
SNPdbers397508301
MSV3drs397508301
GWAS Ctlgrs397508301
Max Magnitude0
ClinVar
Risk rs397508301(;)
Alt rs397508301(;)
Reference rs397508301(GC;GC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232007_117232008delGC
CLNSRC ClinVar
CLNACC RCV000046473.2,