rs35713889

Orientation

plus

Stabilized

plus

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

Make rs35713889(C;T)

Make rs35713889(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

3

Position

49125150

Gene

LAMB2

is a	snp
is	mentioned by
dbSNP	rs35713889
dbSNP (classic)	rs35713889
ClinGen	rs35713889
ebi	rs35713889
HLI	rs35713889
Exac	rs35713889
Gnomad	rs35713889
Varsome	rs35713889
LitVar	rs35713889
Map	rs35713889
PheGenI	rs35713889
Biobank	rs35713889
1000 genomes	rs35713889
hgdp	rs35713889
ensembl	rs35713889
geneview	rs35713889
scholar	rs35713889
google	rs35713889
pharmgkb	rs35713889
gwascentral	rs35713889
openSNP	rs35713889
23andMe	rs35713889
SNPshot	rs35713889
SNPdbe	rs35713889
MSV3d	rs35713889
GWAS Ctlg	rs35713889

Max Magnitude

0

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

[PMID 28146470] Rare and low-frequency coding variants alter human adult height.

ClinVar
Risk	rs35713889(G;G) rs35713889(T;T)
Alt	rs35713889(G;G) rs35713889(T;T)
Reference	Rs35713889(C;C)
Significance	Probable-non-pathogenic
Disease	not specified Pierson syndrome Nephrotic syndrome
Variation	info
Gene	LAMB2
CLNDBN	not specified Pierson syndrome Nephrotic syndrome
Reversed	0
HGVS	NC_000003.11:g.49162583C>T
CLNSRC
CLNACC	RCV000247257.1, RCV000307336.1, RCV000371274.1,