Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.05 (C)
Location

Chromosome 10:37952139 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 synonyms - click the plus to show

This variation has 4 HGVS names - click the plus to show

This variation has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 1863 individual genotypes and is mentioned in 1 citation.

Variation displays