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rs727504040

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504040(G;T)
Make rs727504040(T;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position17376323
GeneNHS
is asnp
is mentioned by
dbSNPrs727504040
ebirs727504040
HLIrs727504040
Exacrs727504040
Varsomers727504040
Maprs727504040
PheGenIrs727504040
hapmaprs727504040
1000 genomesrs727504040
hgdprs727504040
ensemblrs727504040
gopubmedrs727504040
geneviewrs727504040
scholarrs727504040
googlers727504040
pharmgkbrs727504040
gwascentralrs727504040
openSNPrs727504040
23andMers727504040
23andMe allrs727504040
SNP Nexus

SNPshotrs727504040
SNPdbers727504040
MSV3drs727504040
GWAS Ctlgrs727504040
Max Magnitude0
ClinVar
Risk rs727504040(T;T)
Alt rs727504040(T;T)
Reference rs727504040(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NHS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.17394446G>T
CLNSRC
CLNACC RCV000153564.3,