Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C/G | Ancestral: T | Ambiguity code: B

Chromosome 7:55201342 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_042095

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 12 transcripts and has 1 sample genotype.

Variant displays