Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 14:24255457 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981918 ; ESP TMP_ESP_14_24724663_24724663 (C/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 7 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays