Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 6:118559037 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030697

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_110_PLN_172405_0002, 4666

This variation has 12 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays