rs863225287

Orientation

plus

Stabilized

plus

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

Make rs863225287(G;T)

Make rs863225287(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

15

Position

44711614

Gene	B2M, LOC102724979, PATL2

is a	snp
is	mentioned by
dbSNP	rs863225287
dbSNP (classic)	rs863225287
ClinGen	rs863225287
ebi	rs863225287
HLI	rs863225287
Exac	rs863225287
Gnomad	rs863225287
Varsome	rs863225287
LitVar	rs863225287
Map	rs863225287
PheGenI	rs863225287
Biobank	rs863225287
1000 genomes	rs863225287
hgdp	rs863225287
ensembl	rs863225287
geneview	rs863225287
scholar	rs863225287
google	rs863225287
pharmgkb	rs863225287
gwascentral	rs863225287
openSNP	rs863225287
23andMe	rs863225287
SNPshot	rs863225287
SNPdbe	rs863225287
MSV3d	rs863225287
GWAS Ctlg	rs863225287

Max Magnitude

0

ClinVar
Risk	rs863225287(T;T)
Alt	rs863225287(T;T)
Reference	Rs863225287(G;G)
Significance	Pathogenic
Disease	Hypoproteinemia
Variation	info
Gene	B2M
CLNDBN	Hypoproteinemia, hypercatabolic
Reversed	0
HGVS	NC_000015.9:g.45003812G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000201934.2,