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rs727504164

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504164(A;A)
Make rs727504164(A;G)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position53405570
GeneMIR6857, SMC1A
is asnp
is mentioned by
dbSNPrs727504164
ebirs727504164
HLIrs727504164
Exacrs727504164
Varsomers727504164
Maprs727504164
PheGenIrs727504164
hapmaprs727504164
1000 genomesrs727504164
hgdprs727504164
ensemblrs727504164
gopubmedrs727504164
geneviewrs727504164
scholarrs727504164
googlers727504164
pharmgkbrs727504164
gwascentralrs727504164
openSNPrs727504164
23andMers727504164
23andMe allrs727504164
SNP Nexus

SNPshotrs727504164
SNPdbers727504164
MSV3drs727504164
GWAS Ctlgrs727504164
Max Magnitude0
ClinVar
Risk rs727504164(A;A)
Alt rs727504164(A;A)
Reference rs727504164(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MIR6857 SMC1A
CLNDBN not provided
Reversed 1
HGVS NC_000023.10:g.53432502C>T
CLNSRC
CLNACC RCV000153975.3,