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rs7471388

From SNPedia

Orientationplus
Stabilizedplus
Make rs7471388(C;C)
Make rs7471388(C;G)
Make rs7471388(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position71941232
GeneNHSL2
is asnp
is mentioned by
dbSNPrs7471388
ebirs7471388
HLIrs7471388
Exacrs7471388
Varsomers7471388
Maprs7471388
PheGenIrs7471388
hapmaprs7471388
1000 genomesrs7471388
hgdprs7471388
ensemblrs7471388
gopubmedrs7471388
geneviewrs7471388
scholarrs7471388
googlers7471388
pharmgkbrs7471388
gwascentralrs7471388
openSNPrs7471388
23andMers7471388
23andMe allrs7471388
SNP Nexus

SNPshotrs7471388
SNPdbers7471388
MSV3drs7471388
GWAS Ctlgrs7471388
GMAF0.3682
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 22177906] Development of multiplex assay with 16 SNPs on X chromosome for degraded samples