rs121909833

Orientation

plus

Stabilized

plus

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

Make rs121909833(-;-)

Make rs121909833(-;GAA)

Reference

GRCh38 38.1/141

Chromosome

X

Position

152867580

Gene

NSDHL

is a	snp
is	mentioned by
dbSNP	rs121909833
dbSNP (classic)	rs121909833
ClinGen	rs121909833
ebi	rs121909833
HLI	rs121909833
Exac	rs121909833
Gnomad	rs121909833
Varsome	rs121909833
LitVar	rs121909833
Map	rs121909833
PheGenI	rs121909833
Biobank	rs121909833
1000 genomes	rs121909833
hgdp	rs121909833
ensembl	rs121909833
geneview	rs121909833
scholar	rs121909833
google	rs121909833
pharmgkb	rs121909833
gwascentral	rs121909833
openSNP	rs121909833
23andMe	rs121909833
SNPshot	rs121909833
SNPdbe	rs121909833
MSV3d	rs121909833
GWAS Ctlg	rs121909833

Max Magnitude

0

OMIM	300275
Desc
Variant	0008
Related	also

ClinVar
Risk	rs121909833(-;-)
Alt	rs121909833(-;-)
Reference	Rs121909833(GAA;GAA)
Significance	Pathogenic
Disease	NSDHL-Related Disorders
Variation	info
Gene	NSDHL
CLNDBN	NSDHL-Related Disorders
Reversed	0
HGVS	NC_000023.10:g.152036124_152036126delGAA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000020430.11,