rs768785753

Orientation

plus

Stabilized

plus

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

Make rs768785753(C;T)

Make rs768785753(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

183039072

Gene

MCCC1

is a	snp
is	mentioned by
dbSNP	rs768785753
dbSNP (classic)	rs768785753
ClinGen	rs768785753
ebi	rs768785753
HLI	rs768785753
Exac	rs768785753
Gnomad	rs768785753
Varsome	rs768785753
LitVar	rs768785753
Map	rs768785753
PheGenI	rs768785753
Biobank	rs768785753
1000 genomes	rs768785753
hgdp	rs768785753
ensembl	rs768785753
geneview	rs768785753
scholar	rs768785753
google	rs768785753
pharmgkb	rs768785753
gwascentral	rs768785753
openSNP	rs768785753
23andMe	rs768785753
SNPshot	rs768785753
SNPdbe	rs768785753
MSV3d	rs768785753
GWAS Ctlg	rs768785753

Max Magnitude

0

ClinVar
Risk	rs768785753(T;T)
Alt	rs768785753(T;T)
Reference	Rs768785753(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MCCC1
CLNDBN	not provided
Reversed	0
HGVS	NC_000003.11:g.182756860C>T
CLNSRC
CLNACC	RCV000185991.1,