rs104893636

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in complete genomics

Make rs104893636(A;T)

Make rs104893636(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

176151875

Gene	HOXD3, HOXD4

is a	snp
is	mentioned by
dbSNP	rs104893636
dbSNP (classic)	rs104893636
ClinGen	rs104893636
ebi	rs104893636
HLI	rs104893636
Exac	rs104893636
Gnomad	rs104893636
Varsome	rs104893636
LitVar	rs104893636
Map	rs104893636
PheGenI	rs104893636
Biobank	rs104893636
1000 genomes	rs104893636
hgdp	rs104893636
ensembl	rs104893636
geneview	rs104893636
scholar	rs104893636
google	rs104893636
pharmgkb	rs104893636
gwascentral	rs104893636
openSNP	rs104893636
23andMe	rs104893636
SNPshot	rs104893636
SNPdbe	rs104893636
MSV3d	rs104893636
GWAS Ctlg	rs104893636

Max Magnitude

0

OMIM	142981
Desc
Variant	0001
Related	also

ClinVar
Risk	rs104893636(C;C) rs104893636(T;T)
Alt	rs104893636(C;C) rs104893636(T;T)
Reference	Rs104893636(A;A)
Significance	Other
Disease	Leukemia
Variation	info
Gene	HOXD4 HOXD3
CLNDBN	Leukemia, acute lymphoblastic, susceptibility to
Reversed	0
HGVS	NC_000002.11:g.177016603A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000016017.3,