rs1057519877

Orientation

plus

Stabilized

plus

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

Make rs1057519877(A;A)

Make rs1057519877(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

15

Position

44711549

Gene	B2M, LOC102724979, PATL2

is a	snp
is	mentioned by
dbSNP	rs1057519877
dbSNP (classic)	rs1057519877
ClinGen	rs1057519877
ebi	rs1057519877
HLI	rs1057519877
Exac	rs1057519877
Gnomad	rs1057519877
Varsome	rs1057519877
LitVar	rs1057519877
Map	rs1057519877
PheGenI	rs1057519877
Biobank	rs1057519877
1000 genomes	rs1057519877
hgdp	rs1057519877
ensembl	rs1057519877
geneview	rs1057519877
scholar	rs1057519877
google	rs1057519877
pharmgkb	rs1057519877
gwascentral	rs1057519877
openSNP	rs1057519877
23andMe	rs1057519877
SNPshot	rs1057519877
SNPdbe	rs1057519877
MSV3d	rs1057519877
GWAS Ctlg	rs1057519877

Max Magnitude

0

ClinVar
Risk	rs1057519877(A;A)
Alt	rs1057519877(A;A)
Reference	Rs1057519877(G;G)
Significance	Probable-Pathogenic
Disease	Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Malignant lymphoma Malignant melanoma of skin Multiple myeloma Adenocarcinoma of lung Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Small cell lung cancer Squamous cell carcinoma of lung
Variation	info
Gene	B2M
CLNDBN	Colorectal Neoplasms Ovarian Serous Cystadenocarcinoma Malignant lymphoma, non-Hodgkin Malignant melanoma of skin Multiple myeloma Adenocarcinoma of lung Squamous cell carcinoma of the head and neck Adenocarcinoma of stomach Small cell lung cancer Squamous cell carcinoma of lung
Reversed	0
HGVS	NC_000015.9:g.45003747G>A
CLNSRC
CLNACC	RCV000422802.1, RCV000423896.1, RCV000426129.1, RCV000430927.1, RCV000432370.1, RCV000433517.1, RCV000433775.1, RCV000441172.1, RCV000442543.1, RCV000442680.1,