rs769765227

Orientation

plus

Stabilized

plus

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

Make rs769765227(C;T)

Make rs769765227(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

6

Position

31860558

Gene

NEU1

is a	snp
is	mentioned by
dbSNP	rs769765227
dbSNP (classic)	rs769765227
ClinGen	rs769765227
ebi	rs769765227
HLI	rs769765227
Exac	rs769765227
Gnomad	rs769765227
Varsome	rs769765227
LitVar	rs769765227
Map	rs769765227
PheGenI	rs769765227
Biobank	rs769765227
1000 genomes	rs769765227
hgdp	rs769765227
ensembl	rs769765227
geneview	rs769765227
scholar	rs769765227
google	rs769765227
pharmgkb	rs769765227
gwascentral	rs769765227
openSNP	rs769765227
23andMe	rs769765227
SNPshot	rs769765227
SNPdbe	rs769765227
MSV3d	rs769765227
GWAS Ctlg	rs769765227

Max Magnitude

0

ClinVar
Risk	rs769765227(T;T)
Alt	rs769765227(T;T)
Reference	Rs769765227(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NEU1
CLNDBN	not provided
Reversed	0
HGVS	NC_000006.11:g.31828335C>T
CLNSRC
CLNACC	RCV000494284.1,