rs875989786

Orientation

plus

Stabilized

plus

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

Make rs875989786(C;T)

Make rs875989786(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

244054957

Gene

ZBTB18

is a	snp
is	mentioned by
dbSNP	rs875989786
dbSNP (classic)	rs875989786
ClinGen	rs875989786
ebi	rs875989786
HLI	rs875989786
Exac	rs875989786
Gnomad	rs875989786
Varsome	rs875989786
LitVar	rs875989786
Map	rs875989786
PheGenI	rs875989786
Biobank	rs875989786
1000 genomes	rs875989786
hgdp	rs875989786
ensembl	rs875989786
geneview	rs875989786
scholar	rs875989786
google	rs875989786
pharmgkb	rs875989786
gwascentral	rs875989786
openSNP	rs875989786
23andMe	rs875989786
SNPshot	rs875989786
SNPdbe	rs875989786
MSV3d	rs875989786
GWAS Ctlg	rs875989786

Max Magnitude

0

ClinVar
Risk	rs875989786(T;T)
Alt	rs875989786(T;T)
Reference	Rs875989786(C;C)
Significance	Probable-Pathogenic
Disease	Inborn genetic diseases
Variation	info
Gene	ZBTB18
CLNDBN	Inborn genetic diseases
Reversed	0
HGVS	NC_000001.10:g.244218259C>T
CLNSRC
CLNACC	RCV000211094.1,