Variant (rsID / SNP)

rs4988235

rs4988235 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LCT, MCM6. Location: chromosome 2, position 136,608,646. Clinical significance in the table: association.

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Reference-table entries

LCTAssociation

Clinical significance (as recorded): association
Variant type: single nucleotide variant
Chromosome / position: 2:136608646
Cytoband: 2q21.3
HGVS: NM_002299.2(LCT):c.-13907C>T
Allele change: Silent

Associated conditions / phenotypes

Lactase persistence

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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