rs200277996

Orientation

plus

Stabilized

plus

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

Make rs200277996(C;T)

Make rs200277996(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

85514069

Gene

SNX14

is a	snp
is	mentioned by
dbSNP	rs200277996
dbSNP (classic)	rs200277996
ClinGen	rs200277996
ebi	rs200277996
HLI	rs200277996
Exac	rs200277996
Gnomad	rs200277996
Varsome	rs200277996
LitVar	rs200277996
Map	rs200277996
PheGenI	rs200277996
Biobank	rs200277996
1000 genomes	rs200277996
hgdp	rs200277996
ensembl	rs200277996
geneview	rs200277996
scholar	rs200277996
google	rs200277996
pharmgkb	rs200277996
gwascentral	rs200277996
openSNP	rs200277996
23andMe	rs200277996
SNPshot	rs200277996
SNPdbe	rs200277996
MSV3d	rs200277996
GWAS Ctlg	rs200277996

Max Magnitude

0

ClinVar
Risk	rs200277996(T;T)
Alt	rs200277996(T;T)
Reference	Rs200277996(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	SNX14
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.86223787C>T
CLNSRC
CLNACC	RCV000481561.1,