rs2070776

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	2.1	Likely slightly taller - carrier of two alleles for increased height
(C;T)	2	Likely slightly taller - carrier of one allele for increased height
(T;T)	0	common in clinvar

Reference

GRCh38 38.1/141

Chromosome

17

Position

63930138

Gene

CD79B

is a	snp
is	mentioned by
dbSNP	rs2070776
dbSNP (classic)	rs2070776
ClinGen	rs2070776
ebi	rs2070776
HLI	rs2070776
Exac	rs2070776
Gnomad	rs2070776
Varsome	rs2070776
LitVar	rs2070776
Map	rs2070776
PheGenI	rs2070776
Biobank	rs2070776
1000 genomes	rs2070776
hgdp	rs2070776
ensembl	rs2070776
geneview	rs2070776
scholar	rs2070776
google	rs2070776
pharmgkb	rs2070776
gwascentral	rs2070776
openSNP	rs2070776
23andMe	rs2070776
SNPshot	rs2070776
SNPdbe	rs2070776
MSV3d	rs2070776
GWAS Ctlg	rs2070776

GMAF

0.4013

Max Magnitude

2.1

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 20881960]
Trait	Height
Title	Hundreds of variants clustered in genomic loci and biological pathways affect human height.
Risk Allele
P-val	9E-9
Odds Ratio	NR NR

ClinVar
Risk	Rs2070776(C;C)
Alt	Rs2070776(C;C)
Reference	Rs2070776(T;T)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	CD79B
CLNDBN	not specified
Reversed	1
HGVS	NC_000017.10:g.62007498A>G
CLNSRC
CLNACC	RCV000454896.1,