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rs672601316

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs672601316(G;T)
Make rs672601316(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position117592610
GeneCFTR
is asnp
is mentioned by
dbSNPrs672601316
ebirs672601316
HLIrs672601316
Exacrs672601316
Varsomers672601316
Maprs672601316
PheGenIrs672601316
hapmaprs672601316
1000 genomesrs672601316
hgdprs672601316
ensemblrs672601316
gopubmedrs672601316
geneviewrs672601316
scholarrs672601316
googlers672601316
pharmgkbrs672601316
gwascentralrs672601316
openSNPrs672601316
23andMers672601316
23andMe allrs672601316
SNP Nexus

SNPshotrs672601316
SNPdbers672601316
MSV3drs672601316
GWAS Ctlgrs672601316
Max Magnitude0
ClinVar
Risk rs672601316(T;T)
Alt rs672601316(T;T)
Reference rs672601316(G;G)
Significance Pathogenic
Disease Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117232664G>T
CLNSRC
CLNACC RCV000149424.1,