rs1057516387

Orientation

plus

Stabilized

plus

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

Make rs1057516387(-;TC)

Make rs1057516387(TC;TC)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

117540119

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs1057516387
dbSNP (classic)	rs1057516387
ClinGen	rs1057516387
ebi	rs1057516387
HLI	rs1057516387
Exac	rs1057516387
Gnomad	rs1057516387
Varsome	rs1057516387
LitVar	rs1057516387
Map	rs1057516387
PheGenI	rs1057516387
Biobank	rs1057516387
1000 genomes	rs1057516387
hgdp	rs1057516387
ensembl	rs1057516387
geneview	rs1057516387
scholar	rs1057516387
google	rs1057516387
pharmgkb	rs1057516387
gwascentral	rs1057516387
openSNP	rs1057516387
23andMe	rs1057516387
SNPshot	rs1057516387
SNPdbe	rs1057516387
MSV3d	rs1057516387
GWAS Ctlg	rs1057516387

Max Magnitude

0

ClinVar
Risk	rs1057516387(CT;CT)
Alt	rs1057516387(CT;CT)
Reference	Rs1057516387(-;-)
Significance	Probable-Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117180172_117180173dupTC
CLNSRC
CLNACC	RCV000410404.1,