Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.45 (G)
Location

Chromosome 17:42362183 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17593243, rs59978260

This variation has 9 HGVS names - click the plus to show

17:g.42362183A>G
ENST00000585517.2:c.-4-13663T>C
ENST00000588969.2:c.-1-13666T>C
ENST00000404395.3:c.-1-13666T>C
ENST00000588065.1:c.5+11876T>C
ENST00000264657.6:c.-23-13644T>C
ENST00000389272.4:c.-166-15470T>C
LRG_112:g.31313T>C
LRG_112t1.1:c.-23-13644T>C

This variation has assays on 14 chips - click the plus to show

Variation displays