Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 7:139715542 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM054136

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 21 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni5

Variation displays