rs11598702

Orientation

plus

Stabilized

plus

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

Make rs11598702(C;C)

Make rs11598702(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

10

Position

103138228

Gene

NT5C2

is a	snp
is	mentioned by
dbSNP	rs11598702
dbSNP (classic)	rs11598702
ClinGen	rs11598702
ebi	rs11598702
HLI	rs11598702
Exac	rs11598702
Gnomad	rs11598702
Varsome	rs11598702
LitVar	rs11598702
Map	rs11598702
PheGenI	rs11598702
Biobank	rs11598702
1000 genomes	rs11598702
hgdp	rs11598702
ensembl	rs11598702
geneview	rs11598702
scholar	rs11598702
google	rs11598702
pharmgkb	rs11598702
gwascentral	rs11598702
openSNP	rs11598702
23andMe	rs11598702
SNPshot	rs11598702
SNPdbe	rs11598702
MSV3d	rs11598702
GWAS Ctlg	rs11598702

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

ClinVar
Risk	rs11598702(C;C) rs11598702(G;G)
Alt	rs11598702(C;C) rs11598702(G;G)
Reference	Rs11598702(T;T)
Significance	Drug-response
Disease	gemcitabine response - Other
Variation	info
Gene	NT5C2
CLNDBN	gemcitabine response - Other
Reversed	0
HGVS	NC_000010.10:g.104897985T>C
CLNSRC	PharmGKB Clinical Annotation
CLNACC	RCV000211359.1,