rs121909834

Orientation

plus

Stabilized

plus

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

Make rs121909834(-;T)

Make rs121909834(T;T)

Reference

GRCh38 38.1/141

Chromosome

X

Position

152869092

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs121909834
dbSNP (classic)	rs121909834
ClinGen	rs121909834
ebi	rs121909834
HLI	rs121909834
Exac	rs121909834
Gnomad	rs121909834
Varsome	rs121909834
LitVar	rs121909834
Map	rs121909834
PheGenI	rs121909834
Biobank	rs121909834
1000 genomes	rs121909834
hgdp	rs121909834
ensembl	rs121909834
geneview	rs121909834
scholar	rs121909834
google	rs121909834
pharmgkb	rs121909834
gwascentral	rs121909834
openSNP	rs121909834
23andMe	rs121909834
SNPshot	rs121909834
SNPdbe	rs121909834
MSV3d	rs121909834
GWAS Ctlg	rs121909834

Max Magnitude

0

OMIM	300275
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121909834(T;T)
Alt	rs121909834(T;T)
Reference	Rs121909834(-;-)
Significance	Pathogenic
Disease	NSDHL-Related Disorders
Variation	info
Gene	NSDHL
CLNDBN	NSDHL-Related Disorders
Reversed	0
HGVS	NC_000023.10:g.152037636dupT
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000020428.11,