rs397508629

Merged into

rs387906373

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(ATTT;ATTT)	0	common in clinvar
(TATT;TATT)	0	common in clinvar

Make rs397508629(-;-)

Make rs397508629(-;ATTT)

Reference

GRCh38 38.1/141

Chromosome

7

Position

117652851

Gene

CFTR

is a	snp
is	mentioned by
dbSNP	rs397508629
dbSNP (classic)	rs397508629
ClinGen	rs397508629
ebi	rs397508629
HLI	rs397508629
Exac	rs397508629
Gnomad	rs397508629
Varsome	rs397508629
LitVar	rs397508629
Map	rs397508629
PheGenI	rs397508629
Biobank	rs397508629
1000 genomes	rs397508629
hgdp	rs397508629
ensembl	rs397508629
geneview	rs397508629
scholar	rs397508629
google	rs397508629
pharmgkb	rs397508629
gwascentral	rs397508629
openSNP	rs397508629
23andMe	rs397508629
SNPshot	rs397508629
SNPdbe	rs397508629
MSV3d	rs397508629
GWAS Ctlg	rs397508629

Status

Merged into rs387906373

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs397508629(TATT;TATT)
Significance	Pathogenic
Disease	Cystic fibrosis
Variation	info
Gene	CFTR
CLNDBN	Cystic fibrosis
Reversed	0
HGVS	NC_000007.13:g.117292905_117292908delATTT
CLNSRC	CFTR2 OMIM Allelic Variant
CLNACC	RCV000047015.5,