rs121908156

Orientation

minus

Stabilized

minus

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

Make rs121908156(C;T)

Make rs121908156(T;T)

Reference

GRCh38 38.1/141

Chromosome

10

Position

14945110

Gene

DCLRE1C

is a	snp
is	mentioned by
dbSNP	rs121908156
dbSNP (classic)	rs121908156
ClinGen	rs121908156
ebi	rs121908156
HLI	rs121908156
Exac	rs121908156
Gnomad	rs121908156
Varsome	rs121908156
LitVar	rs121908156
Map	rs121908156
PheGenI	rs121908156
Biobank	rs121908156
1000 genomes	rs121908156
hgdp	rs121908156
ensembl	rs121908156
geneview	rs121908156
scholar	rs121908156
google	rs121908156
pharmgkb	rs121908156
gwascentral	rs121908156
openSNP	rs121908156
23andMe	rs121908156
SNPshot	rs121908156
SNPdbe	rs121908156
MSV3d	rs121908156
GWAS Ctlg	rs121908156

Max Magnitude

0

OMIM	605988
Desc
Variant	0001
Related	also

ClinVar
Risk	rs121908156(A;A) rs121908156(T;T)
Alt	rs121908156(A;A) rs121908156(T;T)
Reference	Rs121908156(C;C)
Significance	Pathogenic
Disease	Severe combined immunodeficiency with sensitivity to ionizing radiation not provided
Variation	info
Gene	DCLRE1C
CLNDBN	Severe combined immunodeficiency with sensitivity to ionizing radiation not provided
Reversed	1
HGVS	NC_000010.10:g.14987109G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000004929.4, RCV000224235.2,