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rs727504044

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504044(-;-)
Make rs727504044(-;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position17726739
GeneNHS
is asnp
is mentioned by
dbSNPrs727504044
ebirs727504044
HLIrs727504044
Exacrs727504044
Varsomers727504044
Maprs727504044
PheGenIrs727504044
hapmaprs727504044
1000 genomesrs727504044
hgdprs727504044
ensemblrs727504044
gopubmedrs727504044
geneviewrs727504044
scholarrs727504044
googlers727504044
pharmgkbrs727504044
gwascentralrs727504044
openSNPrs727504044
23andMers727504044
23andMe allrs727504044
SNP Nexus

SNPshotrs727504044
SNPdbers727504044
MSV3drs727504044
GWAS Ctlgrs727504044
Max Magnitude0
ClinVar
Risk rs727504044(;)
Alt rs727504044(;)
Reference rs727504044(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NHS
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.17744859delG
CLNSRC
CLNACC RCV000153569.3,