rs137853148

Orientation

plus

Stabilized

plus

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

Make rs137853148(C;T)

Make rs137853148(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

17589479

Gene

PDGFRL

is a	snp
is	mentioned by
dbSNP	rs137853148
dbSNP (classic)	rs137853148
ClinGen	rs137853148
ebi	rs137853148
HLI	rs137853148
Exac	rs137853148
Gnomad	rs137853148
Varsome	rs137853148
LitVar	rs137853148
Map	rs137853148
PheGenI	rs137853148
Biobank	rs137853148
1000 genomes	rs137853148
hgdp	rs137853148
ensembl	rs137853148
geneview	rs137853148
scholar	rs137853148
google	rs137853148
pharmgkb	rs137853148
gwascentral	rs137853148
openSNP	rs137853148
23andMe	rs137853148
SNPshot	rs137853148
SNPdbe	rs137853148
MSV3d	rs137853148
GWAS Ctlg	rs137853148

Max Magnitude

0

OMIM	604584
Desc
Variant	0001
Related	also

ClinVar
Risk	rs137853148(T;T)
Alt	rs137853148(T;T)
Reference	Rs137853148(C;C)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	PDGFRL
CLNDBN	Carcinoma of colon
Reversed	0
HGVS	NC_000008.10:g.17446988C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000005802.4,