rs786205616

Orientation

minus

Stabilized

minus

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

Make rs786205616(-;-)

Make rs786205616(-;ATCT)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

36592763

Gene	C11orf74, RAG2

is a	snp
is	mentioned by
dbSNP	rs786205616
dbSNP (classic)	rs786205616
ClinGen	rs786205616
ebi	rs786205616
HLI	rs786205616
Exac	rs786205616
Gnomad	rs786205616
Varsome	rs786205616
LitVar	rs786205616
Map	rs786205616
PheGenI	rs786205616
Biobank	rs786205616
1000 genomes	rs786205616
hgdp	rs786205616
ensembl	rs786205616
geneview	rs786205616
scholar	rs786205616
google	rs786205616
pharmgkb	rs786205616
gwascentral	rs786205616
openSNP	rs786205616
23andMe	rs786205616
SNPshot	rs786205616
SNPdbe	rs786205616
MSV3d	rs786205616
GWAS Ctlg	rs786205616

Max Magnitude

0

ClinVar
Risk	rs786205616(-;-)
Alt	rs786205616(-;-)
Reference	Rs786205616(ATCT;ATCT)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	RAG2 C11orf74
CLNDBN	not provided
Reversed	1
HGVS	NC_000011.9:g.36614313_36614316delAGAT
CLNSRC
CLNACC	RCV000171462.1,