Original source

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

C/G | Ancestral: A | Ambiguity code: S | MAF: 0.22 (G)

Chromosome 7:44146206 (forward strand) | View in location tab

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 11 transcripts, has 1097 individual genotypes and is mentioned in 1 citation.

Variation displays