rs1057519879

Orientation

plus

Stabilized

plus

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

Make rs1057519879(C;C)

Make rs1057519879(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

44711548

Gene	B2M, LOC102724979, PATL2

is a	snp
is	mentioned by
dbSNP	rs1057519879
dbSNP (classic)	rs1057519879
ClinGen	rs1057519879
ebi	rs1057519879
HLI	rs1057519879
Exac	rs1057519879
Gnomad	rs1057519879
Varsome	rs1057519879
LitVar	rs1057519879
Map	rs1057519879
PheGenI	rs1057519879
Biobank	rs1057519879
1000 genomes	rs1057519879
hgdp	rs1057519879
ensembl	rs1057519879
geneview	rs1057519879
scholar	rs1057519879
google	rs1057519879
pharmgkb	rs1057519879
gwascentral	rs1057519879
openSNP	rs1057519879
23andMe	rs1057519879
SNPshot	rs1057519879
SNPdbe	rs1057519879
MSV3d	rs1057519879
GWAS Ctlg	rs1057519879

Max Magnitude

0

ClinVar
Risk	rs1057519879(C;C) rs1057519879(G;G)
Alt	rs1057519879(C;C) rs1057519879(G;G)
Reference	Rs1057519879(T;T)
Significance	Probable-Pathogenic
Disease	Adenocarcinoma of lung Multiple myeloma Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Small cell lung cancer Malignant lymphoma Squamous cell carcinoma of lung Adenocarcinoma of stomach Colorectal Neoplasms Malignant melanoma of skin
Variation	info
Gene	B2M
CLNDBN	Adenocarcinoma of lung Multiple myeloma Squamous cell carcinoma of the head and neck Ovarian Serous Cystadenocarcinoma Small cell lung cancer Malignant lymphoma, non-Hodgkin Squamous cell carcinoma of lung Adenocarcinoma of stomach Colorectal Neoplasms Malignant melanoma of skin
Reversed	0
HGVS	NC_000015.9:g.45003746T>C; NC_000015.9:g.45003746T>G
CLNSRC
CLNACC	RCV000419044.1, RCV000419253.1, RCV000420355.1, RCV000426708.1, RCV000427508.1, RCV000429996.1, RCV000437364.1, RCV000438190.1, RCV000439772.1, RCV000444855.1, RCV000421129.1, RCV000421385.1, RCV000423518.1, RCV000428897.1, RCV000432053.1, RCV000434386.1, RCV000434444.1, RCV000438363.1, RCV000439578.1, RCV000442386.1,