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rs397508618

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397508618(-;-)
Make rs397508618(-;C)
ReferenceGRCh38 38.1/141
Chromosome7
Position117642575
GeneCFTR
is asnp
is mentioned by
dbSNPrs397508618
ebirs397508618
HLIrs397508618
Exacrs397508618
Varsomers397508618
Maprs397508618
PheGenIrs397508618
hapmaprs397508618
1000 genomesrs397508618
hgdprs397508618
ensemblrs397508618
gopubmedrs397508618
geneviewrs397508618
scholarrs397508618
googlers397508618
pharmgkbrs397508618
gwascentralrs397508618
openSNPrs397508618
23andMers397508618
23andMe allrs397508618
SNP Nexus

SNPshotrs397508618
SNPdbers397508618
MSV3drs397508618
GWAS Ctlgrs397508618
Max Magnitude0
ClinVar
Risk rs397508618(;)
Alt rs397508618(;)
Reference rs397508618(C;C)
Significance Untested
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117282629delC
CLNSRC ClinVar
CLNACC RCV000046998.2,