rs73715573

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs73715573(G;G)

Make rs73715573(G;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

117548630

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs73715573
dbSNP (classic)	rs73715573
ClinGen	rs73715573
ebi	rs73715573
HLI	rs73715573
Exac	rs73715573
Gnomad	rs73715573
Varsome	rs73715573
LitVar	rs73715573
Map	rs73715573
PheGenI	rs73715573
Biobank	rs73715573
1000 genomes	rs73715573
hgdp	rs73715573
ensembl	rs73715573
geneview	rs73715573
scholar	rs73715573
google	rs73715573
pharmgkb	rs73715573
gwascentral	rs73715573
openSNP	rs73715573
23andMe	rs73715573
SNPshot	rs73715573
SNPdbe	rs73715573
MSV3d	rs73715573
GWAS Ctlg	rs73715573

Max Magnitude

0

ClinVar
Risk	rs73715573(G;G)
Alt	rs73715573(G;G)
Reference	Rs73715573(T;T)
Significance	Other
Disease	Congenital bilateral absence of the vas deferens Cystic fibrosis not provided
Variation	info
Gene	CFTR
CLNDBN	Congenital bilateral absence of the vas deferens Cystic fibrosis not provided
Reversed	0
HGVS	NC_000007.13:g.117188684T>G
CLNSRC
CLNACC	RCV000155471.1, RCV000309488.1, RCV000381834.1,