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rs73715573

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs73715573(G;G)
Make rs73715573(G;T)
ReferenceGRCh38.p2 38.2/144
Chromosome7
Position117548630
GeneCFTR
is asnp
is mentioned by
dbSNPrs73715573
ebirs73715573
HLIrs73715573
Exacrs73715573
Varsomers73715573
Maprs73715573
PheGenIrs73715573
hapmaprs73715573
1000 genomesrs73715573
hgdprs73715573
ensemblrs73715573
gopubmedrs73715573
geneviewrs73715573
scholarrs73715573
googlers73715573
pharmgkbrs73715573
gwascentralrs73715573
openSNPrs73715573
23andMers73715573
23andMe allrs73715573
SNP Nexus

SNPshotrs73715573
SNPdbers73715573
MSV3drs73715573
GWAS Ctlgrs73715573
Max Magnitude0
ClinVar
Risk rs73715573(G;G)
Alt rs73715573(G;G)
Reference rs73715573(T;T)
Significance Probable-Pathogenic
Disease Congenital bilateral absence of the vas deferens Cystic fibrosis
Variation info
Gene CFTR
CLNDBN Congenital bilateral absence of the vas deferens Cystic fibrosis
Reversed 0
HGVS NC_000007.13:g.117188684T>G
CLNSRC
CLNACC RCV000155471.1,