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rs1057519877

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519877(A;A)
Make rs1057519877(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome15
Position44711549
GeneB2M, LOC102724979, PATL2
is asnp
is mentioned by
dbSNPrs1057519877
dbSNP (old)rs1057519877
ClinGenrs1057519877
ebirs1057519877
HLIrs1057519877
Exacrs1057519877
Gnomadrs1057519877
Varsomers1057519877
Maprs1057519877
PheGenIrs1057519877
Biobankrs1057519877
1000 genomesrs1057519877
hgdprs1057519877
ensemblrs1057519877
gopubmedrs1057519877
geneviewrs1057519877
scholarrs1057519877
googlers1057519877
pharmgkbrs1057519877
gwascentralrs1057519877
openSNPrs1057519877
23andMers1057519877
23andMe allrs1057519877
SNPshotrs1057519877
SNPdbers1057519877
MSV3drs1057519877
GWAS Ctlgrs1057519877
Max Magnitude0
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,