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rs397508516

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCTTCCTA;GCTTCCTA) 0 common in clinvar
(TAGCTTCC;TAGCTTCC) 0 common in clinvar
Make rs397508516(-;-)
Make rs397508516(-;GCTTCCTA)
ReferenceGRCh38 38.1/141
Chromosome7
Position117530944
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508516
ebirs397508516
HLIrs397508516
Exacrs397508516
Varsomers397508516
Maprs397508516
PheGenIrs397508516
hapmaprs397508516
1000 genomesrs397508516
hgdprs397508516
ensemblrs397508516
gopubmedrs397508516
geneviewrs397508516
scholarrs397508516
googlers397508516
pharmgkbrs397508516
gwascentralrs397508516
openSNPrs397508516
23andMers397508516
23andMe allrs397508516
SNP Nexus

SNPshotrs397508516
SNPdbers397508516
MSV3drs397508516
GWAS Ctlgrs397508516
Max Magnitude0
ClinVar
Risk rs397508516(;)
Alt rs397508516(;)
Reference rs397508516(TAGCTTCC;TAGCTTCC)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117170998_117171005delGCTTCCTA
CLNSRC ClinVar
CLNACC RCV000046819.2,