rs1057518868

Orientation

plus

Stabilized

plus

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

Make rs1057518868(A;T)

Make rs1057518868(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

16

Position

86510849

Gene	FENDRR, FOXF1

is a	snp
is	mentioned by
dbSNP	rs1057518868
dbSNP (classic)	rs1057518868
ClinGen	rs1057518868
ebi	rs1057518868
HLI	rs1057518868
Exac	rs1057518868
Gnomad	rs1057518868
Varsome	rs1057518868
LitVar	rs1057518868
Map	rs1057518868
PheGenI	rs1057518868
Biobank	rs1057518868
1000 genomes	rs1057518868
hgdp	rs1057518868
ensembl	rs1057518868
geneview	rs1057518868
scholar	rs1057518868
google	rs1057518868
pharmgkb	rs1057518868
gwascentral	rs1057518868
openSNP	rs1057518868
23andMe	rs1057518868
SNPshot	rs1057518868
SNPdbe	rs1057518868
MSV3d	rs1057518868
GWAS Ctlg	rs1057518868

Max Magnitude

0

ClinVar
Risk	rs1057518868(T;T)
Alt	rs1057518868(T;T)
Reference	Rs1057518868(A;A)
Significance	Probable-Pathogenic
Disease	Fetal megacystis Urethral atresia Ventricular septal defect
Variation	info
Gene	FENDRR FOXF1
CLNDBN	Fetal megacystis Urethral atresia Ventricular septal defect
Reversed	0
HGVS	NC_000016.9:g.86544455A>T
CLNSRC
CLNACC	RCV000415110.1,