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rs672601317

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601317(A;A)
Make rs672601317(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position117536634
GeneCFTR
is asnp
is mentioned by
dbSNPrs672601317
ebirs672601317
HLIrs672601317
Exacrs672601317
Varsomers672601317
Maprs672601317
PheGenIrs672601317
hapmaprs672601317
1000 genomesrs672601317
hgdprs672601317
ensemblrs672601317
gopubmedrs672601317
geneviewrs672601317
scholarrs672601317
googlers672601317
pharmgkbrs672601317
gwascentralrs672601317
openSNPrs672601317
23andMers672601317
23andMe allrs672601317
SNP Nexus

SNPshotrs672601317
SNPdbers672601317
MSV3drs672601317
GWAS Ctlgrs672601317
Max Magnitude0
ClinVar
Risk rs672601317(A;A)
Alt rs672601317(A;A)
Reference rs672601317(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117176688G>A
CLNSRC
CLNACC RCV000149425.1,