Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
C/A | Ancestral: A | Ambiguity code: M | MAF: 0.33 (C)
Location

Chromosome 4:38798648 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM073378 ; dbSNP rs76798247 (A/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays