rs1057517068

Orientation

plus

Stabilized

plus

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

Make rs1057517068(-;T)

Make rs1057517068(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

117594993

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs1057517068
dbSNP (classic)	rs1057517068
ClinGen	rs1057517068
ebi	rs1057517068
HLI	rs1057517068
Exac	rs1057517068
Gnomad	rs1057517068
Varsome	rs1057517068
LitVar	rs1057517068
Map	rs1057517068
PheGenI	rs1057517068
Biobank	rs1057517068
1000 genomes	rs1057517068
hgdp	rs1057517068
ensembl	rs1057517068
geneview	rs1057517068
scholar	rs1057517068
google	rs1057517068
pharmgkb	rs1057517068
gwascentral	rs1057517068
openSNP	rs1057517068
23andMe	rs1057517068
SNPshot	rs1057517068
SNPdbe	rs1057517068
MSV3d	rs1057517068
GWAS Ctlg	rs1057517068

Max Magnitude

0

ClinVar
Risk	rs1057517068(T;T)
Alt	rs1057517068(T;T)
Reference	Rs1057517068(-;-)
Significance	Probable-Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117235047dupT
CLNSRC
CLNACC	RCV000411629.1,