rs387907272

Orientation

plus

Stabilized

plus

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

Make rs387907272(C;C)

Make rs387907272(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

38141150

Gene

MYD88

is a	snp
is	mentioned by
dbSNP	rs387907272
dbSNP (classic)	rs387907272
ClinGen	rs387907272
ebi	rs387907272
HLI	rs387907272
Exac	rs387907272
Gnomad	rs387907272
Varsome	rs387907272
LitVar	rs387907272
Map	rs387907272
PheGenI	rs387907272
Biobank	rs387907272
1000 genomes	rs387907272
hgdp	rs387907272
ensembl	rs387907272
geneview	rs387907272
scholar	rs387907272
google	rs387907272
pharmgkb	rs387907272
gwascentral	rs387907272
openSNP	rs387907272
23andMe	rs387907272
SNPshot	rs387907272
SNPdbe	rs387907272
MSV3d	rs387907272
GWAS Ctlg	rs387907272

Max Magnitude

0

ClinVar
Risk	rs387907272(C;C)
Alt	rs387907272(C;C)
Reference	Rs387907272(T;T)
Significance	Pathogenic
Disease	Macroglobulinemia Lymphoma Chronic lymphocytic leukemia Multiple myeloma Malignant lymphoma
Variation	info
Gene	MYD88
CLNDBN	Macroglobulinemia, waldenstrom, somatic Lymphoma Chronic lymphocytic leukemia Multiple myeloma Malignant lymphoma, non-Hodgkin
Reversed	0
HGVS	NC_000003.11:g.38182641T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000030709.6, RCV000425047.1, RCV000431830.1, RCV000442854.1, RCV000443819.1,