rs377729736

Orientation

plus

Stabilized

plus

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

Make rs377729736(A;G)

Make rs377729736(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117531117

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs377729736
dbSNP (classic)	rs377729736
ClinGen	rs377729736
ebi	rs377729736
HLI	rs377729736
Exac	rs377729736
Gnomad	rs377729736
Varsome	rs377729736
LitVar	rs377729736
Map	rs377729736
PheGenI	rs377729736
Biobank	rs377729736
1000 genomes	rs377729736
hgdp	rs377729736
ensembl	rs377729736
geneview	rs377729736
scholar	rs377729736
google	rs377729736
pharmgkb	rs377729736
gwascentral	rs377729736
openSNP	rs377729736
23andMe	rs377729736
SNPshot	rs377729736
SNPdbe	rs377729736
MSV3d	rs377729736
GWAS Ctlg	rs377729736

Max Magnitude

0

ClinVar
Risk	rs377729736(G;G)
Alt	rs377729736(G;G)
Reference	Rs377729736(A;A)
Significance	Untested
Disease	Cystic fibrosis not specified
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis not specified
Reversed	0
HGVS	NC_000007.13:g.117171171A>G
CLNSRC	ClinVar
CLNACC	RCV000047162.3, RCV000401530.1,