rs121909601

Orientation

plus

Stabilized

plus

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

Make rs121909601(A;A)

Make rs121909601(A;G)

Reference

GRCh38 38.1/141

Chromosome

21

Position

33279897

Gene

IL10RB

is a	snp
is	mentioned by
dbSNP	rs121909601
dbSNP (classic)	rs121909601
ClinGen	rs121909601
ebi	rs121909601
HLI	rs121909601
Exac	rs121909601
Gnomad	rs121909601
Varsome	rs121909601
LitVar	rs121909601
Map	rs121909601
PheGenI	rs121909601
Biobank	rs121909601
1000 genomes	rs121909601
hgdp	rs121909601
ensembl	rs121909601
geneview	rs121909601
scholar	rs121909601
google	rs121909601
pharmgkb	rs121909601
gwascentral	rs121909601
openSNP	rs121909601
23andMe	rs121909601
SNPshot	rs121909601
SNPdbe	rs121909601
MSV3d	rs121909601
GWAS Ctlg	rs121909601

Max Magnitude

0

OMIM	123889
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121909601(A;A)
Alt	rs121909601(A;A)
Reference	Rs121909601(G;G)
Significance	Pathogenic
Disease	Inflammatory bowel disease 25
Variation	info
Gene	IL10RB
CLNDBN	Inflammatory bowel disease 25, autosomal recessive
Reversed	0
HGVS	NC_000021.8:g.34652202G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018432.27,