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Variant (rsID / SNP)

rs62618693

QSER1

rs62618693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to QSER1. Location: chromosome 11, position 32,956,492. The table records no clinical significance for this variant.

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Reference-table entries

QSER1Not classified
Variant type
missense_variant
Chromosome / position
11:32956492
HGVS
NM_001076786.3,c.3688C>T,p.Arg1230Cys
Allele change
Missense_R1101C

Associated conditions / phenotypes

Body Mass Index Quantitative Trait Locus 11|Body Mass Index Quantitative Trait Locus 18|Body Mass Index Quantitative Trait Locus 19|Body Mass Index Quantitative Trait Locus 10|Body Mass Index Quantitative Trait Locus 7|Body Mass Index Quantitative Trait Locus 4|Body Mass Index Quantitative Trait Locus 12|Body Mass Index Quantitative Trait Locus 14|Body Mass Index Quantitative Trait Locus 9|Body Mass Index Quantitative Trait Locus 8

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.