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rs10911193

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
(T;T) 1.9
Make rs10911193(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position183021513
GeneLAMC1
is asnp
is mentioned by
dbSNPrs10911193
dbSNP (classic)rs10911193
ClinGenrs10911193
ebirs10911193
HLIrs10911193
Exacrs10911193
Gnomadrs10911193
Varsomers10911193
LitVarrs10911193
Maprs10911193
PheGenIrs10911193
Biobankrs10911193
1000 genomesrs10911193
hgdprs10911193
ensemblrs10911193
geneviewrs10911193
scholarrs10911193
googlers10911193
pharmgkbrs10911193
gwascentralrs10911193
openSNPrs10911193
23andMers10911193
SNPshotrs10911193
SNPdbers10911193
MSV3drs10911193
GWAS Ctlgrs10911193
GMAF0.1189
Max Magnitude1.9
? (C;C) (C;T) (T;T) 28


OMIM176780
DescPELVIC ORGAN PROLAPSE
Variant
Relatedalso
OMIM150290
DescLAMININ, GAMMA-1; LAMC1
Variant
Relatedalso


[PMID 22342894OA-icon.png] Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse


[PMID 17021862] Sequence variant in the laminin gamma1 (LAMC1) gene associated with familial pelvic organ prolapse.


[PMID 20223449OA-icon.png] Is laminin gamma-1 a candidate gene for advanced pelvic organ prolapse?


[PMID 32635941OA-icon.png] Common variants in LAMC1 confer risk for pelvic organ prolapse in Chinese population.