rs1057518121

Orientation

plus

Stabilized

plus

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

Make rs1057518121(C;T)

Make rs1057518121(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

10

Position

248345

Gene	LOC107984190, ZMYND11

is a	snp
is	mentioned by
dbSNP	rs1057518121
dbSNP (classic)	rs1057518121
ClinGen	rs1057518121
ebi	rs1057518121
HLI	rs1057518121
Exac	rs1057518121
Gnomad	rs1057518121
Varsome	rs1057518121
LitVar	rs1057518121
Map	rs1057518121
PheGenI	rs1057518121
Biobank	rs1057518121
1000 genomes	rs1057518121
hgdp	rs1057518121
ensembl	rs1057518121
geneview	rs1057518121
scholar	rs1057518121
google	rs1057518121
pharmgkb	rs1057518121
gwascentral	rs1057518121
openSNP	rs1057518121
23andMe	rs1057518121
SNPshot	rs1057518121
SNPdbe	rs1057518121
MSV3d	rs1057518121
GWAS Ctlg	rs1057518121

Max Magnitude

0

ClinVar
Risk	rs1057518121(T;T)
Alt	rs1057518121(T;T)
Reference	Rs1057518121(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ZMYND11
CLNDBN	not provided
Reversed	0
HGVS	NC_000010.10:g.294285C>T
CLNSRC
CLNACC	RCV000413358.1,